U.S. patent number 10,427,131 [Application Number 15/555,679] was granted by the patent office on 2019-10-01 for guanidine-functionalized perlite particles, articles containing the particles, and methods of using the particles and articles.
This patent grant is currently assigned to 3M Innovative Properties Company. The grantee listed for this patent is 3M INNOVATIVE PROPERTIES COMPANY. Invention is credited to George W. Griesgraber, Manjiri T. Kshirsagar.
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United States Patent |
10,427,131 |
Kshirsagar , et al. |
October 1, 2019 |
**Please see images for:
( Certificate of Correction ) ** |
Guanidine-functionalized perlite particles, articles containing the
particles, and methods of using the particles and articles
Abstract
Guanidine-functionalized perlite particles are provided.
Nonwoven articles are also provided, including a fibrous porous
matrix and guanidine-functionalized perlite particles enmeshed in
the fibrous porous matrix. Laminated articles are additionally
provided, including a first substrate and a second substrate sealed
to the first substrate along at least a portion of a perimeter of
the first substrate. The laminated article further includes
guanidine-functionalized perlite particles disposed between the
first substrate and the second substrate. Methods of detecting
microorganisms or target cellular analytes in a fluid sample using
guanidine-functionalized particles or laminated articles are also
provided.
Inventors: |
Kshirsagar; Manjiri T.
(Woodbury, MN), Griesgraber; George W. (Eagan, MN) |
Applicant: |
Name |
City |
State |
Country |
Type |
3M INNOVATIVE PROPERTIES COMPANY |
St. Paul |
MN |
US |
|
|
Assignee: |
3M Innovative Properties
Company (St. Paul, MN)
|
Family
ID: |
55795166 |
Appl.
No.: |
15/555,679 |
Filed: |
March 15, 2016 |
PCT
Filed: |
March 15, 2016 |
PCT No.: |
PCT/US2016/022409 |
371(c)(1),(2),(4) Date: |
September 05, 2017 |
PCT
Pub. No.: |
WO2016/149233 |
PCT
Pub. Date: |
September 22, 2016 |
Prior Publication Data
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Document
Identifier |
Publication Date |
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US 20180038862 A1 |
Feb 8, 2018 |
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Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
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62135303 |
Mar 19, 2015 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
B01J
20/3204 (20130101); G01N 33/54353 (20130101); B01J
20/28026 (20130101); G01N 33/569 (20130101); G01N
33/56938 (20130101); G01N 33/56916 (20130101); B01J
20/3259 (20130101); G01N 33/54313 (20130101); B01J
20/28035 (20130101); B01J 20/106 (20130101); G01N
33/552 (20130101); B01J 20/22 (20130101) |
Current International
Class: |
B01J
20/10 (20060101); G01N 33/569 (20060101); B01J
20/28 (20060101); B01J 20/22 (20060101); G01N
33/552 (20060101); G01N 33/543 (20060101); B01J
20/32 (20060101) |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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2612854 |
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Jun 2008 |
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CA |
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1989-09279 |
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Oct 1989 |
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WO |
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2010-078404 |
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Jul 2010 |
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WO |
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2011-109151 |
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Sep 2011 |
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WO |
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2014-088807 |
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Jun 2014 |
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WO |
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2015-047464 |
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Apr 2015 |
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WO |
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2015-094938 |
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Jun 2015 |
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WO |
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2016-149235 |
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Sep 2016 |
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WO |
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2016-149472 |
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Sep 2016 |
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WO |
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Other References
`1-Propanarnine,3-(triethoxysilyI)-.` NIST Chemistry WebBook.
[online]. [retrieved on Mar. 31, 2019]. 2018. Retrieved from the
Internet <URL:
https://webbook.nist.gov/cgi/cbook.cgi?ID=919-30-2>. (Year:
2018). cited by examiner .
`N-(2-Arninoethyl)-3-aminopropyltrimethoxysilane`. NIST Chemistry
WebBook. [online]. [retrieved on Mar. 31, 2019]. 2018. Retrieved
from the Internet <
https://webbook.nist.gov/cgi/cbook.cgi?ID=1760-24-3>. (Year:
2018). cited by examiner .
International Search report for PCT International Application No.
PCT/US2016/022409 dated Jun. 26, 2016, 5 pages. cited by
applicant.
|
Primary Examiner: Claytor; Renee
Assistant Examiner: Fernandez; Susan E.
Attorney, Agent or Firm: Pishko; Adrian L.
Parent Case Text
CROSS REFERENCE TO RELATED APPLICATIONS
This application is a national stage filing under 35 U.S.C. 371 of
PCT/US2016/022409, filed Mar. 15, 2016, which claims the benefit of
U.S. Application No. 62/135,303, filed Mar. 19, 2015, the
disclosure of which is incorporated by reference in its/their
entirety herein.
Claims
What is claimed is:
1. A guanidine-functionalized perlite particle comprising a perlite
particle that is modified with at least one silane having the
formula X.sub.3-nR.sup.a.sub.nSi--Y-G, wherein: n is 0, 1, or 2;
each R.sup.a, if present, is independently an alkyl, aralkyl, or
aryl; Y is a divalent group comprising an alkylene having 2 to 20
carbons; G is a guanidine group of the formula
--NH--C(.dbd.NH)--NH.sub.2; and each X is independently alkoxy or
acyloxy.
2. The guanidine-functionalized perlite particle of claim 1,
wherein the divalent group further comprises an arylene, oxy,
--NH--, or a combination thereof.
3. The guanidine-functionalized perlite particle of claim 1,
wherein the divalent group is alkylene having 3 to 6 carbons.
4. The guanidine-functionalized perlite particle of claim 1,
wherein the guanidine group is the reaction product of a primary
amine and an O-methylisourea salt.
5. The guanidine-functionalized perlite particle of claim 4,
wherein the primary amine is 3-aminopropyltrimethoxysilane.
6. The guanidine-functionalized perlite particle of claim 1, having
a surface nitrogen content of at least 2 atomic percent as measured
by x-ray photoelectron spectroscopy (XPS).
7. A nonwoven article comprising a) a fibrous porous matrix and b)
a plurality of guanidine-functionalized perlite particles enmeshed
in the fibrous porous matrix, and wherein each of the
guanidine-functionalized perlite particles comprises a perlite
particle that is modified with at least one silane having the
formula X.sub.3-nR.sup.a.sub.nSi--Y-G, wherein: n is 0, 1, or 2;
each R.sup.a, if present, is independently an alkyl, aralkyl, or
aryl; Y is a divalent group comprising an alkylene having 2 to 20
carbons; G is a guanidine group of the formula
--NH--C(.dbd.NH)--NH.sub.2; and each X is independently alkoxy or
acyloxy.
8. The nonwoven article of claim 7, wherein the fibrous porous
matrix has a thickness of between 0.15 millimeters and 2
millimeters.
9. The nonwoven article of claim 7, wherein the fibrous porous
matrix is a nonwoven fibrous layer comprising polymeric fibers and
inorganic fibers.
10. The nonwoven article of claim 7, wherein the fibrous porous
matrix is a nonwoven fibrous layer and the guanidine-functionalized
perlite particles are distributed throughout the nonwoven fibrous
layer.
11. The nonwoven article of claim 7, wherein the fibrous porous
matrix is a nonwoven fibrous layer comprising uncrimped polymeric
fibers.
12. A laminated article comprising: a. a first substrate; b. a
second substrate sealed to the first substrate along at least a
portion of a perimeter of the first substrate; and c. a plurality
of guanidine-functionalized perlite particles disposed between the
first substrate and the second substrate, wherein each of the
guanidine-functionalized perlite particles comprises a perlite
particle that is modified with at least one silane having the
formula X.sub.3-nR.sup.a.sub.nSi--Y-G, wherein: n is 0, 1, or 2;
each R.sup.a, if present, is independently an alkyl, aralkyl, or
aryl; Y is a divalent group comprising an alkylene having 2 to 20
carbons; G is a guanidine group of the formula
--NH--C(.dbd.NH)--NH.sub.2; and each X is independently alkoxy or
acyloxy.
13. The laminated article of claim 12, wherein the first substrate
and the second substrate are independently selected from a spunbond
polypropylene, a spunbond polyamide, a spunbond blend of polyamide
and polyester, a spunbond polyethylene, a spunbond polyester, a
spunbond polybutylene terephthalate, and a spunbond
polypropylene.
14. A method of detecting microorganisms or target cellular
analytes in a fluid sample, the method comprising: a) providing a
laminated article according to claim 12; b) providing a fluid
sample suspected of containing at least one microorganism strain or
target cellular analyte; c) contacting the fluid sample with the
laminated article such that at least a portion of the at least one
microorganism strain or target cellular analyte is bound to the
laminated article; and d) detecting the presence of the at least
one bound microorganism strain or bound target cellular
analyte.
15. The method of claim 14, wherein the detecting comprises a
bioluminescence method.
16. The method of claim 14, wherein the bound target cellular
analyte comprises a nucleic acid, a protein, a cell wall component,
ATP, or a combination thereof.
17. The method of claim 14, wherein the contacting comprises
passing the fluid sample through the laminated article at a
pressure of 4.0 pounds per square inch (psi) (27.58 kilopascals
(kPa)) or less.
18. A method of detecting microorganisms or target cellular
analytes in a fluid sample, the method comprising: a) providing a
plurality of guanidine-functionalized perlite particles according
to claim 1; b) providing a fluid sample suspected of containing at
least one microorganism strain or target cellular analyte; c)
contacting the fluid sample with the plurality of
guanidine-functionalized perlite particles such that at least a
portion of the at least one microorganism strain or target cellular
analyte is bound to the guanidine-functionalized perlite particles;
and d) detecting the presence of the at least one bound
microorganism strain or bound target cellular analyte.
Description
FIELD
The present disclosure relates to guanidine-functionalized perlite
particles, nonwoven articles, laminated articles, and methods of
using the particles, nonwoven articles, and laminated articles,
such as for detecting microorganisms in a fluid sample.
BACKGROUND
It is often desirable or necessary to assay for the presence of
bacteria or other microorganisms in various clinical, food,
environmental, or other samples, in order to determine the identity
and/or the quantity of the microorganisms present. Bacterial DNA or
bacterial RNA, for example, can be assayed to assess the presence
or absence of a particular bacterial species even in the presence
of other bacterial species. The ability to detect the presence of a
particular bacterium, however, depends, at least in part, on the
concentration of the bacterium in the sample being analyzed.
Concentration of the bacteria in the sample can shorten the
culturing time or even eliminate the need for a culturing step.
Thus, methods have been developed to isolate (and thereby
concentrate) particular bacterial strains by using antibodies
specific to the strain (for example, in the form of antibody-coated
magnetic or non-magnetic particles). Such methods, however, have
tended to be expensive and still somewhat slower than desired for
at least some diagnostic applications. Non-specific concentration
or capture of microorganisms has been achieved through methods
based upon carbohydrate and lectin protein interactions. Various
inorganic materials (for example, hydroxyapatite and metal
hydroxides) have also been used to non-specifically bind and
concentrate bacteria. Such non-specific concentration methods have
varied in speed, cost, sample requirements, space requirements,
ease of use, suitability for on-site use, and/or effectiveness.
Rapid methods based on ATP bioluminescence assays have been used to
determine microbial contamination in water as they provide
immediate results; however, the methods are limited by detection
sensitivity because they require at least 1.times.10.sup.5 colony
forming units (cfu)/ml to elicit detectable responses. One can
increase the sensitivity of the ATP bioluminescence assay by using
a larger volume of sample (e.g., 100 ml), but such methods can be
difficult to implement in the field.
SUMMARY
Guanidine-functionalized perlite particles are provided, as well as
nonwoven articles and laminated articles containing the particles,
which can be used to detect microorganisms and/or cellular analytes
in fluid samples.
In a first aspect, a guanidine-functionalized perlite particle is
provided. The guanidine-functionalized perlite particle includes a
perlite particle that is modified with at least one silane having
the formula X.sub.3-nR.sup.a.sub.nSi--Y-G. In the formula, n is 0,
1, or 2 and each R.sup.a, if present, is independently an alkyl,
aralkyl, or aryl. In the formula, Y is a divalent group comprising
an alkylene having 2 to 20 carbons, G is a guanidine group of the
formula --NH--C(.dbd.NH)--NH.sub.2, and each X is independently
alkoxy or acyloxy.
In a second aspect, a nonwoven article is provided. The nonwoven
article includes a fibrous porous matrix and a plurality of
guanidine-functionalized perlite particles enmeshed in the fibrous
porous matrix.
In a third aspect, a laminated article is provided. The laminated
article includes a first substrate and a second substrate sealed to
the first substrate along at least a portion of a perimeter of the
first substrate. The laminated article further includes a plurality
of guanidine-functionalized perlite particles disposed between the
first substrate and the second substrate.
In a fourth aspect, a method of detecting microorganisms or target
cellular analytes in a fluid sample is provided. The method
includes providing a laminated article according to the third
aspect and providing a fluid sample suspected of containing at
least one microorganism strain or target cellular analyte. The
method further includes contacting the fluid sample with the
laminated article such that at least a portion of the at least one
microorganism strain or target cellular analyte is bound to the
laminated article and detecting the presence of the at least one
bound microorganism strain or bound target cellular analyte.
In a fifth aspect, another method of detecting microorganisms or
target cellular analytes in a fluid sample is provided. The method
includes providing a plurality of guanidine-functionalized perlite
particles according to the second aspect and providing a fluid
sample suspected of containing at least one microorganism strain or
target cellular analyte. The method further includes contacting the
fluid sample with the plurality of guanidine-functionalized perlite
particles such that at least a portion of the at least one
microorganism strain or target cellular analyte is bound to the
guanidine-functionalized perlite particles and detecting the
presence of the at least one bound microorganism strain or bound
target cellular analyte.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a scanning electron microscope (SEM) image of the
exemplary guanidine-functionalized perlite particles of Example
1.
FIG. 2 is an SEM image of the exemplary nonwoven article of Example
3.
DETAILED DESCRIPTION
Guanidine-functionalized perlite particles, nonwoven articles and
laminated articles including the particles, and rapid methods for
monitoring of microbial content of fluid samples are provided. The
guanidine-functionalized particles concentrate at least one
microorganism or target cellular analyte and allow detection of the
bound microorganism or target cellular analyte. The
guanidine-functionalized particles, nonwoven articles, and
laminated articles may be contacted with large volumes of fluid
samples to concentrate the microorganism and/or target cellular
analyte, and also allow further optional washing to remove
contaminants prior to detection. Methods according to the
disclosure are capable of readily detecting bacterial contamination
in fluid samples in about 15 minutes. Accordingly, the
guanidine-functionalized particles, nonwoven articles, laminated
articles, and methods can be suitable for field based detection of
microorganisms and target cellular analytes in fluid samples.
For the following Glossary of defined terms, these definitions
shall be applied for the entire application, unless a different
definition is provided in the claims or elsewhere in the
specification.
Glossary
Certain terms are used throughout the description and the claims
that, while for the most part are well known, may require some
explanation. It should be understood that, as used herein:
The term "a", "an", and "the" are used interchangeably with "at
least one" to mean one or more of the elements being described. The
term "and/or" means either or both. For example "A and/or B" means
only A, only B, or both A and B.
As used in this specification, the recitation of numerical ranges
by endpoints includes all numbers subsumed within that range (e.g.
1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.8, 4, and 5).
Unless otherwise indicated, all numbers expressing quantities or
ingredients, measurement of properties and so forth used in the
specification and embodiments are to be understood as being
modified in all instances by the term "about." Accordingly, unless
indicated to the contrary, the numerical parameters set forth in
the foregoing specification and attached listing of embodiments can
vary depending upon the desired properties sought to be obtained by
those skilled in the art utilizing the teachings of the present
disclosure. At the very least, and not as an attempt to limit the
application of the doctrine of equivalents to the scope of the
claimed embodiments, each numerical parameter should at least be
construed in light of the number of reported significant digits and
by applying ordinary rounding techniques.
The term "comprises" and variations thereof do not have a limiting
meaning where these terms appear in the description and claims.
The term "consists essentially of" does not exclude the presence of
additional materials which do not significantly affect the desired
characteristics of a given composition or product.
The words "preferred" and "preferably" refer to embodiments of the
disclosure that may afford certain benefits, under certain
circumstances. However, other embodiments may also be preferred,
under the same or other circumstances. Furthermore, the recitation
of one or more preferred embodiments does not imply that other
embodiments are not useful, and is not intended to exclude other
embodiments from the scope of the disclosure.
The term "acyloxy" refers to a monovalent group of formula --O(CO)R
where R is an alkyl group.
The term "alkoxy" refers to a monovalent group of formula --OR
where R is an alkyl group.
The term "alkyl" refers to a monovalent group that is a radical of
an alkane and includes groups that are linear, branched, cyclic, or
combination thereof. The alkyl group typically has 1 to 30 carbon
atoms. In some embodiments, the alkyl group contains 1 to 20 carbon
atoms, 1 to 10 carbon atoms, 1 to 6 carbon atoms, or 1 to 4 carbon
atoms. Examples of alkyl groups include, but are not limited to,
methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl,
n-pentyl, n-hexyl, cyclohexyl, n-heptyl, n-octyl, and
ethylhexyl.
The term "alkylene" refers to a divalent group that is a radical of
an alkane. The alkylene can be straight-chained, branched, cyclic,
or combination thereof. The alkylene typically has 1 to 200 carbon
atoms. In some embodiments, the alkylene contains 1 to 100, 1 to
80, 1 to 50, 1 to 30, 1 to 20, 1 to 10, or 1 to 4 carbon atoms. The
radical centers of the alkylene can be on the same carbon atom
(i.e., an alkylidene) or on different carbon atoms.
The term "aralkyl" refers to a monovalent group that is a radical
of the compound R--Ar where Ar is an aromatic carbocyclic group and
R is an alkyl group.
The term "aryl" refers to a monovalent group that is a radical of a
carbocyclic aromatic compound. The aryl can have one aromatic ring
or can include up to 5 other carbocyclic rings that are connected
to or fused to the aromatic ring. The other carbocyclic rings can
be aromatic, non-aromatic, or combination thereof. Examples of aryl
groups include, but are not limited to, phenyl, biphenyl,
terphenyl, anthryl, naphthyl, acenaphthyl, anthraquinonyl,
phenanthryl, anthracenyl, pyrenyl, perylenyl, and fluorenyl.
The term "cellular analyte" means an analyte of cellular origin
(that is, a microorganism or a component thereof (for example, a
cell or a cellular component such as deoxyribonucleic acid (DNA) or
ribonucleic acid (RNA), proteins, nucleotides such as adenosine
triphosphate (ATP), and the like, and combinations thereof);
references to a microorganism or microorganism strain throughout
this specification are meant to apply more generally to any
cellular analyte).
The term "concentration agent" means a material or composition that
binds microorganisms and/or cellular analytes from a fluid sample
(preferably, having a cellular analyte capture or binding
efficiency of at least about 60 percent, or at least about 70
percent, or at least about 80 percent, or at least about 90
percent), thereby concentrating the microorganisms and/or cellular
analytes into a smaller volume than when present in the fluid
sample. The concentration agent according to this disclosure
comprises guanidine-functionalized perlite particles.
The term "detection" means the identification of a microorganism or
of a cellular analyte (for example, at least a component of a
target microorganism, which thereby determines that the target
microorganism is present).
The term "enmeshed" (in regard to particles in a fibrous porous
matrix) means that the particles are entrapped in and on the
fibrous porous matrix (and, preferably, distributed within it),
rather than solely being borne on its surface.
The term "fibrillated" (in regard to fibers or fibrous material)
means treated (for example, by beating) in a manner that forms
fibrils or branches attached to a fiber's main trunk.
The term "fibrous porous matrix" means a nonwoven web or medium,
(i.e., not a woven or knitted fabric), comprising interlaid fibers,
for example, a web comprising fibers that are interlaid by
meltblowing, spunbonding, or other air laying techniques; carding;
wet laying; or the like. Typically, the fibers have lengths of less
than 100 millimeters and are uncrimped.
The term "filtering" is generally used to describe the process of
separating matter by size, charge and/or function. For example,
filtering can include separating soluble matter and a solvent
(e.g., diluent) from insoluble matter, or it can include separating
soluble matter, a solvent and relatively small insoluble matter
from relatively large insoluble matter. A variety of filtration
methods can be used, including, but not limited to, passing the
liquid composition through a filter, settling followed by
aspiration or decanting, other suitable filtration methods, and
combinations thereof "Settling" is used to refer to allowing the
insoluble matter in the liquid composition to settle. Settling may
occur by gravity or by centrifugation. The insoluble matter (or
relatively large insoluble matter) can then be separated from the
soluble matter (or soluble matter and relatively small insoluble
matter) and solvent by aspirating the soluble matter and solvent
from the insoluble matter, decanting the soluble matter and
solvent, or a combination thereof.
The term "filtrate" is generally used to describe the liquid
remaining after the insoluble matter (or at least the relatively
large insoluble matter) has been removed from the liquid
composition.
The term "fluid" means liquid, solution, or dispersion of solid or
liquid in liquid.
The term "laminated" means an article having a plurality of stacked
layers (for example, an article having a first substrate layer, a
particle layer disposed on the first substrate layer, and a second
substrate layer disposed on the particle layer).
The term "microorganism" means any cell or particle having genetic
material suitable for analysis or detection (including, for
example, bacteria, yeasts, viruses, and bacterial endospores).
The term "microorganism strain" means a particular type of
microorganism that is distinguishable through a detection method
(for example, microorganisms of different genera, of different
species within a genera, or of different isolates within a
species).
The term "polygon" means a shape having three or more sides.
The terms "polymer" and "polymeric material" are used
interchangeably and refer to materials formed by reacting one or
more monomers.
The term "sample" means a substance or material that is collected
(for example, to be analyzed).
The term "sample matrix" means the components of a sample other
than microorganisms and/or cellular analytes.
The term "target cellular analyte" means any cellular analyte that
is desired to be detected.
The term "target microorganism" means any microorganism that is
desired to be detected.
The term "through pore" (in reference to a porous matrix) means a
pore that comprises a passageway or channel (with separate inlet
and outlet) through the porous matrix.
Reference throughout this specification to "one embodiment,"
"certain embodiments," "one or more embodiments" or "an
embodiment," whether or not including the term "exemplary"
preceding the term "embodiment," means that a particular feature,
structure, material, or characteristic described in connection with
the embodiment is included in at least one embodiment of the
certain exemplary embodiments of the present disclosure. Thus, the
appearances of the phrases such as "in one or more embodiments,"
"in some embodiments," "in certain embodiments," "in one
embodiment," "in many embodiments" or "in an embodiment" in various
places throughout this specification are not necessarily referring
to the same embodiment of the certain exemplary embodiments of the
present disclosure. Furthermore, the particular features,
structures, materials, or characteristics may be combined in any
suitable manner in one or more embodiments.
Various exemplary embodiments of the disclosure will now be
described. Exemplary embodiments of the present disclosure may take
on various modifications and alterations without departing from the
spirit and scope of the disclosure. Accordingly, it is to be
understood that the embodiments of the present disclosure are not
to be limited to the following described exemplary embodiments, but
are to be controlled by the limitations set forth in the claims and
any equivalents thereof.
In a first aspect, a guanidine-functionalized perlite particle is
provided. The guanidine-functionalized perlite particle includes a
perlite particle that is modified with at least one
guanidine-containing ligand. Perlite is a naturally-forming
amorphous volcanic glass, containing about 70-75% silicon dioxide
and 12-15% aluminum oxide, as well as smaller amounts of other
metal oxides, including sodium oxide, potassium oxide, iron oxide,
magnesium oxide, and calcium oxide. When perlite is expanded by
heat it forms a lightweight aggregate, to about four to twenty
times its initial volume. Perlite has been used in applications
such as construction applications (e.g., as an insulator or
texturizer), horticultural applications (e.g., to provide aeration
and moisture retention or as a carrier for fertilizer or other
active agents), and industrial applications (e.g., as an abrasive,
filler, or filter media for water and other fluid samples).
Examples of suitable perlite particles include the 4106 grade
material, 4156 grade material, and the 476 grade material, both
commercially available from Dicaperl Minerals Corporation
(Crawfordsville, Ind.).
The guanidine-containing ligand is formed by modifying the perlite
particle with a guanidine-containing silane having the structure
shown in Formula 1: X.sub.3-nR.sup.a.sub.nSi--Y-G Formula 1
In Formula 1, Si is a silicon atom, and G denotes a guanidine group
of the formula --NH--C(.dbd.NH)--NH.sub.2. Y is a divalent group
that is covalently bonded to the silicon atom at one end and to the
G group at the other end. Each R.sup.a group, if any are present,
is independently an alkyl, aralkyl, or aryl group, and is attached
to the silicon atom. Each X is a leaving group covalently bonded to
the silicon atom and is independently alkoxy or acyloxy, and n is
0, 1, or 2.
A typical alkylene can be up to 20, up to 16, 12, 10, 8, 7, 6, 5,
4, or even up to 3 carbons, or even 2 carbons, inclusive of the
terminal atoms of the divalent group. In some embodiments, Y is a
divalent group comprising an alkylene of 3 to 6 carbons. In a
preferred embodiment, Y is a divalent group having 3 carbons (i.e.,
propyl).
In Formula 1, each leaving group X is independently an alkoxy group
of 1, 2, 3, 4, 5, 6, 7, 8, 9, or even up to 10 carbons, or is an
acyloxy group of 2 carbons, or 3, 4, 5, 6, 7, 8, 9, or even up to
10 carbons, where the alkoxy or acyloxy group is bonded to the
silicon through an oxygen atom.
In some embodiments, n is 0. When n is 0, no R.sup.a groups are
present, and Formula 1 can be re-written more simply as shown in
Formula 2 (where Si, G, Y, and X are as defined for Formula 1):
X.sub.3Si--Y-G Formula 2
When the silane of Formula 1 (or Formula 2) reacts with an --OH
group on the surface of a perlite particle, at least one X leaving
group is replaced by a covalent bond of between the silicon atom
and an oxygen atom on the surface of the perlite particle. An
embodiment of a guanidine-functionalized perlite particle
comprising a specific exemplary guanidine-containing ligand within
the general type represented by Formula 1, wherein n=0 (i.e., as in
Formula 2), is shown in Formula 3 (the circle in Formula 3
represents a perlite particle):
##STR00001##
It will be understood that Formula 3 represents a specific
embodiment wherein n is 3 and Y is a divalent group that is
alkylene having 3 carbons. In each of Formulas 1 to 3, the
ionization state of the guanidine group is omitted; however, it
will be understood that in various environments such guanidine
groups may be charged or uncharged (e.g., protonated or
deprotonated), for example, according to the pH of a liquid medium
in which the guanidine group is present, as discussed later
herein.
The covalent bond(s) between the oxygen(s) of the ligand and the
particle can be conveniently obtained, for example, by reacting a
Si-bonded hydrolyzable group of the guanidine-containing precursor
with a hydroxyl group of the particle, as discussed in detail later
herein. While the exemplary structure of Formula 3 shows three such
bonded oxygen atoms (i.e., n=3 in Formula 1), it will be
appreciated that in various embodiments one, two or three such
bonded oxygen atoms can be provided. If less than three such oxygen
atoms are bonded to the silicon atom, other substituents (e.g.,
substituents that are not bonded to the particle, and which are not
shown in Formula 1) may be present on the silicon atom. For
example, the guanidine-containing ligand can include a polymeric
structure involving formation of Si--O--Si (i.e., siloxane) groups,
resulting from Si--O bonds being formed between two or more
guanidine-containing ligand precursors. Without being bound by
theory, it is thought that Si--O--Si groups may form in the
presence of added water, or other aqueous solvents, or other agent
that can hydrolyze bonds in Si--O--R groups, to give rise to more
complex guanidine-containing ligand structures attached to
particles, including such possible structures as shown in the
non-limiting examples of Formulas 4a to 4d (each R in Formulas 4a
to 4d independently being H or lower alkyl (e.g., methyl), or even
another Si atom in which may or may not be attached to the perlite
particle through an Si--O-- bond; the circle in each of Formulas 4a
to 4d represents a perlite particle):
##STR00002## ##STR00003##
It is seen from Formulas 4a to 4d that a network of polymerized
guanidine-containing ligands can form a coating on the surface of
the perlite particle. In some embodiments it may be desirable to
obtain the particle functionalized with polymerized
guanidine-containing ligand (e.g., as in any of the non-limiting
polymerized guanidine-containing ligand structures shown in
Formulas 4a to 4d, or the like, having at least one Si--O--Si group
in the polymerized guanidine-containing ligand), as a means of
increasing the loading of nitrogen-containing guanidine groups on
the surface of the perlite particle. It is thought that in at least
these types of polymerizations, a loading of nitrogen-containing
guanidine groups on the surface of the perlite particle can attain
levels of surface nitrogen content in a range from 1 to 10 atomic
percent, as can be measured, for example, by X-ray photoelectron
spectroscopy.
Concentration agent particles are water-insoluble particulate
materials that have been employed to non-specifically capture
microorganism strains, cellular analytes, or a combination thereof,
when contacted with fluid samples containing microorganisms and/or
cellular analytes. The concentration agent particles typically
comprise microparticles.
The guanidine-functionalized perlite particles used in nonwoven
articles of the present disclosure can be used in essentially any
particulate form (preferably, a relatively dry or volatiles-free
form) that is amenable to blending with fibers to form the nonwoven
articles of the present disclosure, or amenable to encapsulating
between two substrates to form the laminated articles of the
present disclosure. Preferably, the guanidine-functionalized
perlite particles are used in the form of a powder. Useful powders
include those that comprise microparticles (preferably,
microparticles having a particle size in the range of about 1
micrometer (more preferably, about 2 micrometers; even more
preferably, about 3 micrometers; most preferably, about 4
micrometers) to about 100 micrometers (more preferably, about 50
micrometers; even more preferably, about 25 micrometers; most
preferably, about 15 or 20 micrometers; where any lower limit can
be paired with any upper limit of the range, as referenced
above).
X-ray photoelectron spectroscopy ("XPS", also known as Electron
Spectroscopy for Chemical Analysis ("ESCA")) is a technique that
can provide information about the elemental and chemical (oxidation
state and/or functional group) concentrations present on a solid
surface. XPS typically provides an analysis of the outermost 3 to
10 nanometers (nm) of the specimen surface. XPS is sensitive to all
elements in the periodic table except hydrogen and helium with
detection limits for most species in the 0.1 to 1 atomic percent
concentration range. In some cases, for example for perlite
particles, a preferred surface composition assessment conditions
for XPS can include a take-off angle of 45 degrees measured with
respect to the sample surface with a solid angle of acceptance of
.+-.20 degrees. A person skilled in the art can select a suitable
instrument setting for analysis of particles of the present
disclosure. Suitable guanidine-functionalized perlite particles for
use according to the present disclosure include those that comprise
perlite and that have a surface composition having a surface
nitrogen content of greater than 2 and less than or equal to about
12, as determined by XPS.
It will be appreciated that a guanidine group as described herein
may be uncharged or charged (e.g., protonated) depending on the
particular environment in which it is placed (e.g., depending on
the pH of an aqueous buffer with which the guanidine-functionalized
particle is brought into contact). In environments in which a
guanidine group of a guanidine-functionalized particle is charged,
the charged guanidine group may comprise an associated counterion.
In some embodiments such a counterion may arise in the generation
of the guanidine group (that is, the guanidine group as produced in
the synthesis reaction may be charged, and may have a counterion
associated therewith, as discussed later herein). In other
embodiments a counterion may not arise in the generation of the
guanidine group (e.g., the guanidine group may be produced in the
synthesis reaction as a free base), but the guanidine-containing
ligand (e.g., the functionalized particle) may be later placed into
an environment (e.g., a liquid buffer) in which the guanidine group
becomes charged and a corresponding counterion becomes associated
therewith. In still other embodiments, a particular counterion may
be associated with the guanidine group (e.g. as synthesized), but
the counterion may then be exchanged for a different counterion.
The charge state of a guanidine group and the presence and identity
and charge state of a counterion thus possibly varying with
environment, it is emphasized that all references to guanidine
groups in the claims herein, are irrespective of the charge state
of the guanidine group and are irrespective of the presence or
identity of an associated counterion, unless such charge state
and/or presence and/or identity of a counterion is explicitly
specified in the claim.
Furthermore, the concept of a counterion that is associated with a
guanidine group is used broadly herein, and it will be understood
that such a counterion may not necessarily be constantly located in
close proximity to the same guanidine group. Furthermore, the
guanidine group and the associated counterion do not necessarily
have to always be fully solvated (e.g., in aqueous solution). That
is, they may be present as salts in a partially or substantially
dried product (e.g., a solid or semi-solid product), which product
may be placed into a liquid (e.g., an aqueous buffer) and solvated
as desired. In specific embodiments, the associated counterion is a
sulfate and/or bisulfate ion. In other specific embodiments, the
associated counterion is a hydroxide ion (as may result, for
example, from putting a guanidine group in the free-base form into
an unbuffered aqueous solution).
In some embodiments, a guanidine-functionalized particle can be
made by a simple and convenient method using an O-alkylisourea, or
a salt thereof (for example, O-methylisourea hemisulfate, which is
a readily available starting material, CAS No. 52328-05-9). In a
first step of this method, an O-alkylisourea may be reacted with a
linker molecule of the general structure shown in Formula 5:
X.sub.3-nR.sup.a.sub.nSi--Y--NH.sub.2 Formula 5
In Formula 5, Si is a silicon atom, and NH.sub.2 denotes a primary
amino group. Y is a divalent group that is covalently bonded to the
silicon atom at one end and to the primary amino group at the other
end. Each R.sup.a group, if any are present, is independently an
alkyl, aralkyl, or aryl group, and is attached to the silicon atom
(noting that no R.sup.a group will be present when n is 0). Each X
is a leaving group covalently bonded to the silicon atom and is
independently alkoxy or acyloxy, and n is 0, 1, or 2.
In some embodiments, Y is a divalent alkylene group. A typical
alkylene can be up to 20, up to 16, 12, 10, 8, 7, 6, 5, 4, or even
up to 3 carbons, or even 2 carbons. In some embodiments, Y is a
divalent group comprising an alkylene of 3 to 6 carbons. In a
preferred embodiment, Y is a divalent group having 3 carbons (i.e.,
propyl), as shown, for example in the preferred linker compound of
Formula 6.
##STR00004##
In some embodiments, a first step of a method of making a
guanidine-functionalized perlite particle is shown in Reaction
Scheme 1, reacting a compound of Formula 5 with an O-alkylisourea
(R' can be methyl or other lower alkyl, including anywhere from 2
to 10 carbons). The reaction can be carried out in a suitable
solvent (e.g., methanol or ethanol).
##STR00005##
In a more specific embodiment of Reaction Scheme I, the compound of
Formula 6 is reacted with an O-methylisourea salt, as shown in
Reaction Scheme II.
##STR00006##
In Reaction Scheme II, O-methylisourea is provided as a
hemisulfate, and is reacted with 3-aminopropyltrimethoxysilane (in
methanol) to form the guanidine group (noting that the charge state
of the guanidine group and of the associated hemisulfate counterion
are not shown in Reaction Scheme II).
It will be appreciated that Formula 6 and Reaction Scheme II are
representative examples and that any suitable linker molecule can
be used (as long as the linker molecule includes, e.g., a primary
amine that can be reacted with the O-methylisourea to form a
guanidine group), within the overall boundaries prescribed herein.
For example, the linker molecule can comprise any desired number of
any suitable reactive groups (e.g., ethoxy, methoxy, acetoxy) on
the silicon atom (noting that if multiple reactive groups are
present they do not have to be identical; further noting that if
less than three such reactive groups are used, other (e.g.,
R.sup.a) groups can be present, e.g. as shown in the general
representation of Formula 4, and still further noting that if
multiple R.sup.a groups are present they do not have to be
identical). In a specific example, 3-aminopropyltriethoxysilane may
be used as the linker molecule rather than the
3-aminopropyltrimethoxysilane of Formula 6 and included in Reaction
Scheme II.
In some embodiments, Y is a divalent group comprising an alkylene,
and the divalent group can further optionally comprise other
groups, including an arylene, oxy, --NH--, or a combination
thereof. In some specific embodiments, the divalent Y group of the
linker molecule may comprise a secondary amine. In a particular
example of this type, the linker molecule may be e.g.
N-(2-aminoethyl)-3-aminopropyltrimethoxysilane (available under the
trade designation "SIA0591.0" from Gelest, Inc., Tullytown, Pa.).
Other potentially useful linker molecules may include e.g.
(aminoethylaminomethyl) phenethyltrimethoxysilane ("SIA0588.0",
Gelest), N-(2-aminoethyl)-3-aminopropylmethyldimethoxysilane
("SIA0589.0", Gelest), N-(6-aminohexyl) aminopropyltrimethoxysilane
("SIA0594.0", Gelest),
N-(2-aminoethyl)-11-aminoundecyl-trimethoxysilane ("SIA0595.0",
Gelest), N-3[(amino(polypropylenoxy)]aminopropyltrimethoxysilane
("SIA0599.4", Gelest), 3-aminopropylmethyldiethoxysilane
("SIA0605.0", Gelest), 3-aminopropyltriethoxysilane ("SIA0610.0",
Gelest), and (3-trimethoxysilylpropyl)diethylene-triamine
("SIT8398.0", Gelest). Mixtures of any of the herein-mentioned
linker molecules may be used if desired.
In a second step of this method, at least one of the Si-bonded X
groups of the linker molecule (with Si atoms comprising one or more
such reactive alkoxy or acyloxy groups being well known by the term
silane coupling agents) is reacted with a hydroxyl group of a
suitable particle to form a covalent bond between the linker
molecule and the particle. (It is emphasized that the terminology
of "first" and "second" steps is used purely for convenience of
description and that the steps can be performed in any desired
order). For example, any or all of the three trimethoxy reactive
groups of the linker molecule in Reaction Scheme II may react with
surface hydroxyl groups of the particle. In some embodiments, and
as mentioned above, the addition of water in the second step of
this method has been observed to result in higher surface nitrogen
values as measured by XPS (see Example section). The amount of
water added can be in a range from 0 to 5 equivalents ("eq") of
water relative to the amount of linker molecule ("equivalents" here
refers to "molar equivalents", defined as 1 mole of water for each
1 mole of linker molecule), which can include up to 1 eq, or up to
2 eq, up to 1 eq, up to 0.5 eq, up to 0.25 eq, or even any value in
between 0 eq and 5 eq of water, relative the amount of linker
molecule.
In one embodiment, the net result of these two steps is summarized
in exemplary embodiment in Formula 7 (the circle in Formula 7
represents a perlite particle):
##STR00007##
The specific exemplary representation of Formula 7 shows the
thus-produced guanidine group in a positively charged (e.g.,
protonated) condition with a negatively charged hemisulfate
counterion associated therewith. It will be understood that a
guanidine-functionalized particle may be produced in such condition
by the above method, but that the charge state of the guanidine
group, the presence, identity and/or charge state of a counterion,
etc., may be affected thereafter by the environment into which the
guanidine-functionalized particle is placed, as discussed
above.
The general methods-of-making described above, and materials used
therein, may be tailored as desired for particular purposes. Thus,
in some embodiments, each thus-formed guanidine-containing ligand
on the particle may only have a single guanidine group (rather than
there being e.g. two, three or more guanidine groups on a given
guanidine-containing ligand). In some embodiments, the thus-formed
guanidine-comprising ligands may be the only ligands on the
particle (rather than there being additional ligands, e.g.
silane-coupled ligands, on the particle, which additional ligands
do not comprise a guanidine group). In some embodiments, a
substantial amount (e.g., an amount readily detectable by surface
analysis) of residual hydroxyls are present on the surface of the
particle even after the attachment of the linker molecules to some
of the hydroxyls of the particle to form ligands thereon (e.g.,
rather than the residual hydroxyls being endcapped). In some
embodiments, the methods disclosed herein do not include a step of
equilibrating the particle in an atmosphere having a defined
relatively humidity (e.g., of less than 40%) prior to the reacting
of the linker molecule with a surface hydroxyl group of the
particle. While the method outlined in Reaction Scheme II uses an
O-methylisourea, it will be appreciated that other starting
materials might be used to make a guanidine-functionalized linker
of the general structure of Formula 1. Such starting materials
might include e.g. O-alkylisourea salts such as O-methylisourea
sulfate, O-methylisourea hydrogen sulfate, O-methylisourea acetate,
O-ethylisourea hydrogen sulfate, and O-ethylisourea hydrochloride.
Beyond these materials, other starting materials that might be used
to make a guanidine-functionalized linker of the general structure
of Formula 1 might include e.g. cyanamide, chloroformamidine
hydrochloride; 1-amidino-1,2,4-triazole hydrochloride;
3,5-dimethylpyrazole-1-carboxamidine nitrate;
pyrazole-1-carboxamidine hydrochloride;
N-amidinopyrazole-1-carboxamidine hydrochloride. It will be
appreciated that some of these starting materials may produce a
guanidine-containing linker in which the guanidine group is in a
specific charge state (e.g., is a free base or is positively
charged) and/or has a specific counterion associated therewith. It
will be understood that such a guanidine group may be placed into a
specific charge state, may have its associated counterion exchanged
for some other counterion, and so on, based on the disclosures
herein.
In a second aspect, a nonwoven article is provided. The nonwoven
article includes a fibrous porous matrix and a plurality of
guanidine-functionalized perlite particles enmeshed in the fibrous
porous matrix. The nonwoven fibrous porous matrix is often in the
form of a layer of interlaid fibers that are not woven or knitted
together. The nonwoven, fibrous porous matrix can be prepared by
any suitable process such as, for example, air laying techniques,
spunlaid techniques such as meltblowing or spunbonding, carding,
wetlaying, and combinations thereof. In many embodiments, the
fibrous nonwoven matrix is prepared by wetlaid techniques.
Fibers suitable for use in preparing the nonwoven fibrous porous
matrix are usually pulpable or extrudable fibers such as those that
are stable to radiation and/or to a variety of solvents.
Optionally, at least some of the polymeric fibers can be selected
to exhibit a degree of hydrophilicity. Useful fibers include
polymeric fibers, inorganic fibers, and combinations thereof. More
particularly, the fibers include a plurality of different types of
fibers, including polyolefin fibers and fiberglass fibers.
Suitable polymeric fibers include those made from natural polymers
(those derived from animal or vegetable sources) and/or synthetic
polymers, including thermoplastic and solvent-dispersible polymers.
Useful polymers include polyolefins (for example, poly(ethylene)
(e.g., low density polyethylene, medium density polyethylene, high
density polyethylene, etc.), polypropylene, poly(1-butene),
copolymers of ethylene and propylene, alpha olefin copolymers such
as copolymers of ethylene or propylene with 1-butene, 1-hexene,
1-octene, and 1-decene such as poly(ethylene-co-1-butene),
poly(ethylene-co-1-butene-co-1-hexene), and the like); polylactic
acid; poly(isoprenes); poly(butadienes); polyamides (for example,
nylon 6, nylon 6,6, nylon 6,12,
poly(iminoadipoyliminohexamethylene),
poly(iminoadipoyliminodecamethylene), polycaprolactam, and the
like); polyimides (for example, poly(pyromellitimide) and the
like); polyethers; poly(ether sulfones) (for example,
poly(diphenylether sulfone), poly(diphenylsulfone-co-diphenylene
oxide sulfone), and the like); poly(sulfones); poly(vinyl esters)
such as poly(vinyl acetates); copolymers of vinyl acetate (for
example, poly(ethylene-co-vinyl acetate), copolymers in which at
least some of the acetate groups have been hydrolyzed to provide
various poly(vinyl alcohols) including poly(ethylene-co-vinyl
alcohol), and the like); poly(phosphazenes); poly(vinyl ethers);
poly(vinyl alcohols); polyaramids (for example, para-aramids such
as poly(paraphenylene terephthalamide) and fibers sold under the
trade designation "KEVLAR" by DuPont Co., Wilmington, Del., pulps
of which are commercially available in various grades based on the
length of the fibers that make up the pulp such as, for example,
"KEVLAR 1F306" and "KEVLAR 1F694", both of which include aramid
fibers that are at least 4 mm in length; and the like); wool; silk;
cellulosic polymers (for example, cellulose, cellulose derivatives
such as rayon, and the like); acrylic polymers (for example,
polyacrylonitrile); polyesters (for example, polyethylene
terephthalate); fluorinated polymers (for example, poly(vinyl
fluoride), poly(vinylidene fluoride), copolymers of vinylidene
fluoride such as poly(vinylidene fluoride-co-hexafluoropropylene),
copolymers of chlorotrifluoroethylene such as
poly(ethylene-co-chlorotrifluoroethylene), and the like);
chlorinated polymers; poly(carbonates); and the like; and
combinations thereof. In certain embodiments, the polymeric fibers
comprise a polyolefin, a polysulfone, a polyamide, or a combination
thereof.
Suitable inorganic fibers include those that contain at least one
inorganic material selected from glasses, ceramics, and
combinations thereof. These fibers are often added to provide
strength to the fibrous porous matrix. For example, porous matrix
layers containing inorganic fibers are often capable of being bent,
folded, or pleated without breaking apart. Useful inorganic fibers
include, for example, fiberglass (for example, E-glass, S-glass,
and the like), ceramic fibers (for example, fibers made of metal
oxides (such as alumina), silicon carbide, boron nitride, boron
carbide, and the like), and combinations thereof. Useful ceramic
fibers can be at least partially crystalline (exhibiting a
discernible X-ray powder diffraction pattern or containing both
crystalline and amorphous (glass) phases). In some applications,
the inorganic fibers include fiberglass.
To facilitate entrapment of the guanidine-functionalized perlite
particles and/or to ensure a high surface area, the fibers used to
form the nonwoven, fibrous porous matrix often contain at least one
fibrillated fiber (for example, in the form of a main fiber
surrounded by many smaller attached fibrils). The main fiber
generally can have a length in the range of 0.5 millimeters to 5
millimeters and a diameter in a range of 1 micrometer to 20
micrometers. The fibrils typically can have a sub-micrometer
diameter. In many embodiments, the fibrillated fibers are prepared
from a polyolefin such as poly(ethylene) or polypropylene, or from
an acrylic polymer such as polyacrylonitrile.
Suitable polymeric fibers further include bi-component fibers,
which typically assist in binding all of the matrix fibers together
due to a difference in melting point of one of the materials in the
bi-component fiber. Bi-component fibers can have, for example, a
core-sheath structure, a side-by-side structure, an
islands-in-the-sea structure, or a segmented-pie structure, or the
like. An example side-by-side bi-component fiber is the polyolefin
thermally bonded bi-component fiber that is commercially available
from Chisso Corporation (Osaka, Japan) under the trade designation
CHISSO (for example, CHISSO ES). An example core-sheath
bi-component fiber is commercially available from Unitika Ltd.
(Osaka, Japan) under the trade designation MELTY (for example,
MELTY 4080) and those commercially available from Minifibers, Inc.
(Johnson City, Tenn.) made of ethyl vinyl acetate (sheath) and
polypropylene (core), or made of a co-polyester of polyester and
polyethylene terephthalate (PET) (sheath) and polyester (core).
The nonwoven fibrous porous matrix contains a plurality of
different types of fibers. In some embodiments, the porous matrix
can be formed using three, four, or even more different types of
fibers. For example, a fiberglass fiber can be added for strength
and integrity, while fibrillated poly(ethylene) can be added for
entrapment of the particulates. Additionally, nylon fibers provide
hydrophilic character while fibrillated poly(ethylene) fibers
provide hydrophobic character to the porous matrix. If fibrillated
and non-fibrillated fibers are used in combination, the weight
ratio of fibrillated fibers to non-fibrillated fibers is often at
least 1:2, at least 1:1, at least 2:1, at least 3:1, at least 5:1,
or even at least 8:1. In some embodiments, mixtures of hydrophobic
and hydrophilic polymeric fibers are used. For example, the fibrous
porous matrix can include a mixture of hydrophobic fibers such as
polyolefins plus hydrophilic fibers such as polysulfones. In some
specific examples, the polymeric fibers include polyolefin fibers,
bi-component fibers, and fiberglass fibers.
In certain embodiments, the fibrous porous matrix is free of
polyamide fibers. It has been discovered that the inclusion of
nylon fibers in the fibrous porous matrix can result in lower
luminescence than the fibrous porous matrix without the nylon
fibers for a bioluminescent ATP detection method.
Preferably, the fibers used to form the nonwoven fibrous porous
matrix are uncrimped. In contrast to uncrimped fibers, crimped
fibers may be identified as displaying repeating features (as
manifested e.g., in a wavy, jagged, sinusoidal, etc., appearance of
the fiber), by having a helical appearance (e.g., particularly in
the case of crimped fibers obtained by thermal activation of
bi-component fibers), and the like, and are readily recognizable by
those of ordinary skill in the art. Exemplary crimped fibers are
described in U.S. Pat. No. 4,118,531 to Hauser and U.S. Pat. No.
5,597,645 to Pike et al., and CA Patent 2612854 to Sommer et
al.
The fibers used to form the nonwoven fibrous porous matrix can be
of a length and diameter that can provide a porous matrix having
sufficient structural integrity and sufficient porosity for a
particular application (for example, passing a fluid sample through
the matrix). The fiber lengths are often at least about 0.5
millimeter, at least 1 millimeter, at least 2 millimeters, at least
3 millimeters, at least 4 millimeters, at least 6 millimeters, at
least 8 millimeters, at least 10 millimeters, at least 15
millimeters, or at least 20 millimeters, and up to 50 millimeters,
up to 40 millimeters, up to 30 millimeters, or up to 25
millimeters. The diameter of the fibers can be, for example, at
least 10 micrometers, at least 20 micrometers, or at least 30
micrometers. The fiber lengths and diameters will vary depending
upon factors such as the nature of the fiber and the type of
application.
The nonwoven fibrous porous matrix often includes a mixture of
polyolefin fibers, glass fibers, and bi-component fibers. In some
particular embodiments, the nonwoven fibrous porous matrix contains
a mixture of fibrillated polyethylene fibers, glass fibers, and
sheath-core bi-component fibers. In some examples, the nonwoven
fibrous porous matrix contains 40 to 80 weight percent fibrillated
polyethylene fibers, 5 to 20 weight percent glass fibers, and 5 to
20 weight percent bi-component fibers. In some examples, the
nonwoven fibrous porous matrix contains 40 to 80 weight percent
fibrillated polyethylene fibers, 10 to 30 weight percent nylon
fibers, 5 to 20 weight percent glass fibers, and 5 to 20 weight
percent bi-component fibers. In other examples, the nonwoven,
fibrous porous matrix contains 50 to 70 weight percent fibrillated
polyethylene fibers, 5 to 15 weight percent glass fibers, and 5 to
20 weight percent bi-component fibers. In still other examples, the
fibrous porous matrix contains 55 to 65 weight percent fibrillated
polyethylene fibers, 0 to 20 weight percent nylon fibers, 5 to 15
weight percent glass fibers, and 10 to 20 weight percent
bi-component fibers.
As noted above, the fibrous porous matrix consists essentially of
inorganic fibers and polymeric fibers. Accordingly, in most
embodiments, the fibrous porous matrix contains only fibers. For
example, at least 90 weight percent, at least 95 weight percent, at
least 98 weight percent, at least 99 weight percent, or at least
99.5 weight percent of a dry fibrous porous matrix is fibers. In
certain embodiments, the nonwoven article comprises a thickness of
at least 0.1 millimeters, or at least 0.15 millimeters, or at least
0.2 millimeters, or at least 0.3 millimeters, or at least 0.4
millimeters, or at least 0.5 millimeters, or at least 0.6
millimeters. The nonwoven article usually comprises a thickness of
up to 1 millimeter, or up to 0.9 millimeters, or up to 0.8
millimeters, or up to 0.7 millimeters, or up to 0.55 millimeters.
Stated differently, the nonwoven article may comprise a thickness
of between 0.15 millimeters and 1 millimeter, or between 0.15
millimeters and 0.8 millimeters, or between 0.1 millimeters and 0.7
millimeters. In certain embodiments, a nonwoven article having a
thickness towards the lower end of the thickness range is selected
to minimize interference with detection of the microorganisms
and/or cellular analytes, such as decreasing time required for a
reagent to diffuse into the nonwoven article, or decreasing
blockage of a generated detection signal.
The nonwoven article typically includes both the fibrous porous
matrix and guanidine-functionalized perlite particles distributed
within the fibrous porous matrix. In most embodiments, the nonwoven
article contains at least 10 weight percent
guanidine-functionalized perlite particles based on a total dry
weight of the nonwoven article. If the amount of the
guanidine-functionalized perlite particles is lower than about 10
weight percent, the nonwoven article may not contain enough
guanidine-functionalized perlite particles to effectively capture
microorganisms or cellular analytes from a fluid sample. In some
examples, the nonwoven article contains at least 15 weight percent,
at least 20 weight percent, at least 25 weight percent, or at least
30 weight percent guanidine-functionalized perlite particles based
on a total dry weight of the nonwoven article.
On the other hand, the nonwoven article usually contains no greater
than 55 weight percent guanidine-functionalized perlite particles
based on the total dry weight of the nonwoven article. If the
amount of the guanidine-functionalized perlite particles is greater
than about 55 weight percent, the nonwoven article may contain an
insufficient amount of the fibrous porous matrix. That is, the
strength of the nonwoven article may be insufficient to hold
together when employed to capture microorganism strains and/or
target cellular analytes. In some examples, the nonwoven article
contains no greater than 50 weight percent, no greater than 45
weight percent, or no greater than 40 weight percent
guanidine-functionalized perlite particles based on a total weight
of the nonwoven article.
Stated differently, the nonwoven article often contains 10 to 55
weight percent guanidine-functionalized perlite particles and 45 to
90 weight percent fibrous porous matrix, 15 to 50 weight percent
guanidine-functionalized perlite particles and 50 to 85 weight
percent fibrous porous matrix, 20 to 50 weight percent
guanidine-functionalized perlite particles and 50 to 80 weight
percent fibrous porous matrix, 20 to 45 weight percent
guanidine-functionalized perlite particles and 55 to 80 weight
percent fibrous porous matrix, 25 to 40 weight percent
guanidine-functionalized perlite particles and 60 to 75 weight
percent fibrous porous matrix, or 30 to 40 weight percent
guanidine-functionalized perlite particles and 60 to 70 weight
percent fibrous porous matrix. The amounts are based on the total
dry weight of the nonwoven article.
In many embodiments, the nonwoven article (when dry) contains only
guanidine-functionalized perlite particles and fibrous porous
matrix. For example, the nonwoven article contains at least 90
weight percent, at least 95 weight percent, at least 98 weight
percent, at least 99 weight percent, or at least 99.5 weight
percent combined guanidine-functionalized perlite particles and
fibrous porous matrix when dry.
In one specific method, a nonwoven article is prepared using a wet
laying or "wetlaid" process. In this process, a dispersion is
formed that contains (a) a plurality of fibers, (b) a plurality of
guanidine-functionalized perlite particles, (c) polymeric binder
fibers, (d) and a dispersing liquid such as water, a water-miscible
organic solvent, or a mixture thereof. The fibers and
guanidine-functionalized perlite particles can be dispersed
together in the dispersing liquid. In some embodiments, the fibers
(for example, hydrophobic fibers) have additives, surface
treatments, or chemical groups that facilitate dispersion of the
fibers in the dispersion liquid. For example, polyolefin-based
fibers can have maleic anhydride or succinic anhydride
functionality, or, during the melt-processing to prepare
polyolefin-based fibers, a suitable surfactant can be added.
The wetlaid process additionally includes dewatering, followed by
heating to finish the dewatering and optionally to bind some of the
fibers together.
One or more adjuvants or additives are optionally used in preparing
this type of nonwoven article. Useful adjuvants include process
aids, surfactants, solvents, dispersants, flocculating aids,
retention aids, or other materials that can enhance the overall
performance of the resulting nonwoven article. When used, the
amounts of such adjuvants can be present, for example, in an amount
up 5 weight percent, up to 4 weight percent, up to 3 weight
percent, up to 1 weight percent, or up to 0.5 weight percent based
on a total dry weight of the nonwoven article (for example, fibers
and guanidine-functionalized perlite particles). The total amount
of adjuvants is typically selected to be as low as possible so as
to maximize the amount of guanidine-functionalized perlite
particles that can be included in the nonwoven article.
In one more specific wetlaid process, the fibers (for example,
chopped fibers) can be blended in a container in the presence of
the dispersing liquid (for example, water, a water-miscible organic
solvent such as an alcohol, or a mixture thereof) to form a slurry.
After formation of the slurry, the guanidine-functionalized perlite
particles and an optional precipitation agent (for example, a pH
adjusting agent such as alum) can be added to the slurry.
When the wetlaid process is carried out by using hand-sheet methods
known in the art, the order of addition of the components (i.e.,
fibers and guanidine-functionalized perlite particles) to the
dispersion has not been found to significantly affect the ultimate
performance of the nonwoven article. After formation, the
dispersion mixture can be poured into a mold, the bottom of which
can be covered by a screen. The dispersing liquid can be allowed to
drain from the mixture (in the form of a wet sheet) through the
screen. After sufficient liquid has drained, the wet sheet
generally can be removed from the mold and dried by pressing,
heating, or a combination of the two. Generally pressures are in a
range of about 300 to about 600 kPa. Temperatures in a range of
90.degree. C. to 200.degree. C., in a range of 100.degree. C. to
175.degree. C., in a range of 100.degree. C. to 150.degree. C., or
in a range of 90.degree. C. to 120.degree. C. can be used for
drying the wet sheet. Drying often removes all or most of the
dispersing liquid (for example, up to 85 weight percent, up to 90
weight percent, up to 95 weight percent, up to 98 weight percent,
or up to 99 weight percent of the dispersing liquid based on the
amount of dispersing liquid added to form the dispersion).
The resulting nonwoven article is a dry sheet having an average
thickness of at least 0.1 millimeter, at least 0.2 millimeters, at
least 0.5 millimeters, at least 0.8 millimeters, at least 1
millimeter, at least 2 millimeters, at least 4 millimeters, or at
least 5 millimeters. The average thickness is often up to 20
millimeters, up to 15 millimeters, up to 12 millimeters, or up to
10 millimeters. Calendering can be used to provide additional
pressing or fusing, if desired, of the dry sheet. The basis weight
of the nonwoven article (in the form of sheet material) can be in
the range of about 100 to about 350 grams per square meter
(g/m.sup.2), preferably, in the range of about 200 to about 300
g/m.sup.2, such as about 250 g/m.sup.2.
In the nonwoven article, the guanidine-functionalized perlite
particles can be entrapped in the fibrous porous matrix through
either chemical interactions (for example, chemical bonding) or
physical interactions (for example, adsorption or mechanical
entrapment), depending upon the nature of the fibers that are
utilized. The guanidine-functionalized perlite particles are often
preferably distributed essentially uniformly throughout the fibrous
porous matrix within the nonwoven article.
Generally the average pore size of the dry nonwoven article can be
in a range of 0.1 to 10 micrometers, as measured by scanning
electron microscopy (SEM). Void volumes in the range of 20 to 80
volume percent or in a range of 40 to 60 volume percent can be
useful. The porosity of the dry nonwoven article can be modified
(increased) by using fibers of larger diameter or stiffness in the
fiber mixture.
In a third aspect, a laminated article is provided. The laminated
article includes a first substrate and a second substrate sealed to
the first substrate along at least a portion of a perimeter of the
first substrate. The laminated article further includes a plurality
of guanidine-functionalized perlite particles disposed between the
first substrate and the second substrate.
Substrates that are suitable for laminated articles of the present
disclosure include a spunbond polypropylene, a spunbond blend of
polyamide and polyester, a spunbond polyamide, a spunbond
polyethylene, a spunbond polyester, a spunbond polybutylene
terephthalate (PBT), a spunbond polypropylene, a melt-blown web, a
staple web, and most preferably a spunbond polypropylene or a
spunbond blend of polyamide and polyester. Preferably, each of the
first substrate and the second substrate are selected from
materials that shed few or no fibers, such that the turbidity of a
fluid sample passed through the laminated article is not detectably
increased as compared to the turbidity of the fluid sample prior to
being passed through the laminated article, or passes the Turbidity
Test described below. The first substrate and the second substrate
are independently selected from suitable materials, but often
include the same material. It is emphasized that the terminology of
"first" and "second" substrates is used purely for convenience of
description; in certain embodiments, the first substrate and the
second substrate are portions of a single continuous substrate,
whereas in alternate embodiments the first substrate and the second
substrate are individual, separate, substrates. One example of the
first substrate and the second substrate being portions of a single
continuous substrate, for instance, is a substrate folded in half
wherein one half provides the first substrate while the other half
provides the second substrate.
To allow flow of a liquid (e.g., a fluid sample) through the
thickness of the laminated article, each of the first substrate and
the second substrate is fluid permeable. In many applications,
fluids comprising water (e.g., aqueous solutions or dispersions)
will be passed through the laminated article, thus optionally at
least one of the first substrate and the second substrate comprise
a hydrophilized substrate to improve wettability and penetration of
the liquid through one or both substrates. Hydrophilization is well
known to the skilled practitioner, and may be performed using
plasma treatment, for instance (see, e.g., U.S. Pat. No.
4,772,488).
Characteristics of spunbond materials typically correlated to
porosity include the basis weight of a unit area of the material
and the diameter of the individual fibers of which the spunbond
materials are composed. Suitable substrates for laminated articles
according to the present disclosure include one or more spunbond
materials comprising a gram per square meter basis weight (gsm) of
at least about 10, 25, 40, 55, 60, or even 65 gsm up to about 75,
80, 90, 100, 140, 180, or even 200 gsm. For example, in certain
aspects, the first substrate and the second substrate independently
include a spunbond material comprising a gsm of 10 to 200 gsm,
preferably 55 to 100 gsm, and most preferably 60 to 100 gsm,
inclusive. In certain aspects, the first substrate and the second
substrate independently comprise a spunbond material comprising a
fiber diameter of at least about 10 micrometers (.mu.m), 11, 12,
13, 14, or even 15 .mu.m up to about 17, 18, 19, 20, 22, 24, 26,
28, or even 30 .mu.m. For example, in certain aspects, the first
substrate and the second substrate independently comprise a
spunbond material comprising a fiber diameter of 10 to 30 .mu.m,
and preferably 10 to 18 .mu.m, 12 to 20 .mu.m, or 14 to 22 .mu.m,
inclusive.
Laminated articles of the present disclosure include a seal to
secure the first substrate to the second substrate. In particular,
the second substrate is sealed to the first substrate along at
least a portion of the perimeter of the substrate. As used herein,
the term "perimeter" means the border or outer boundary of a
substrate, including all of the area within about 10% of the
distance of the furthest edge of the border or outer boundary
inward towards the center of the substrate. For instance, if a
substrate comprises a circular shape having a radius of 10
centimeters (cm), the perimeter includes any of the area from the
outer edge to 1 cm in from the outer edge toward the center of the
circular shape. Alternatively, if a substrate comprises a rectangle
(e.g., polygon) shape having a length of 40 cm and a height of 20
cm, the perimeter includes any of the area from the outer edges of
the short ends to 4 cm in towards the center point of the rectangle
and from the outer edges of the long ends to 2 cm in towards the
center point of the rectangle. Typically, the second substrate is
sealed to the first substrate along at least about 75%, or 85%, or
90% of the perimeter of the first substrate, and up to about 95%,
or 98%, or 100% of the perimeter of the first substrate. In
addition to the sealing along at least a portion of the perimeter
of the first substrate, point bonding (or pin bonding) of discreet
points inward of the perimeter of the first substrate is optionally
also employed. An advantage of performing point bonding is
providing further stability of the guanidine-functionalized perlite
particles remaining where they were originally disposed between the
first and second substrates.
Sealing of the first substrate to the second substrate may be
accomplished by various suitable methods known in the art,
including for example and without limitation, ultrasonic sealing,
heat sealing, adhesive sealing, stitching, or a combination
thereof. Ultrasonic sealing may be a preferred method, and is
typically performed at an energy setting of at least about 150
joules (J), or 175 J, or 200 J, or even 225 J, up to about 200 J,
225 J, or even 250 J, for example 150 J to 250 J, inclusive. In
certain embodiments, the ultrasonic sealing simultaneously seals
and cuts the laminated article in a single step, eliminating the
need for individually separating the laminated article from the
substrate material.
Laminated articles of the present disclosure can be prepared by a
process comprising (a) providing a plurality of the above-described
guanidine-functionalized perlite particles; (b) providing the
above-described first substrate; (c) providing the above-described
second substrate; (d) disposing the guanidine-functionalized
perlite particles between the first substrate and the second
substrate; and (e) sealing the second substrate to the first
substrate along at least a portion of a perimeter of the first
substrate (as described above).
In a fourth aspect, a method of detecting microorganisms or target
cellular analytes in a fluid sample is provided. The method
includes providing a laminated article according to the third
aspect (as described above) and providing a fluid sample suspected
of containing at least one microorganism strain or target cellular
analyte. The method further includes contacting the fluid sample
with the laminated article such that at least a portion of the at
least one microorganism strain or target cellular analyte is bound
to the laminated article and detecting the presence of the at least
one bound microorganism strain or bound target cellular
analyte.
The methods according to the present disclosure can be carried out
by any of various known or hereafter-developed methods of providing
contact between two materials. For example, the laminated article
or nonwoven article can be added to the fluid sample, or the fluid
sample can be added to the articles. For instance, sample can be
passed over or through (preferably, through) the laminated article
or nonwoven article. For the nonwoven article, the contacting is
optionally carried out in a manner such that the sample passes
through a pore of the fibrous porous matrix (such as a through
pore). For the laminated article, the contacting is optionally
carried out in a manner such that the sample passes through the
first substrate, past at least one guanidine-functionalized perlite
particle, and the second substrate. In an embodiment of the present
disclosure, a filtration device is includes a container having
inlet and outlet ports for liquid passage, and a laminated article
or nonwoven article of the present disclosure contained within the
container.
Contacting can be carried out for a desired period (for example,
for sample volumes of several liters or for processes involving
multiple passes through a laminated article or nonwoven article, up
to about 60 minutes of contacting can be useful, or about 15
seconds to about 30 minutes, or about 15 seconds to about 15
minutes, or about 15 second to about 10 minutes, or about 15
seconds to about 5 minutes, or even about 15 seconds to about 2
minutes).
Contacting can be effected by passing a sample at least once
(preferably, only once) through a laminated article or nonwoven
article (for example, by gravity, by vacuum, or by pumping).
Essentially any type of pump (for example, a peristaltic pump) or
other equipment for establishing a pressure differential across a
sample of the nonwoven article or laminated article contained in a
suitable container having inlet and outlet ports for liquid passage
(for example, a syringe or plunger) can be utilized. Useful flow
rates will vary, depending upon such factors as the nature of the
fluid sample matrix and the particular application. Advantageously,
the nonwoven articles and laminated articles of the present
disclosure require only a very low pressure differential across the
articles to effectively pass a fluid sample through the articles.
This characteristic is particularly beneficial in environments, for
instance, when no or low power pumps are available for processing a
fluid sample, or in dealing with complex sample matrices such as
industrial water samples. In an embodiment of the present
disclosure, the contacting comprises passing the fluid sample
through the nonwoven article or laminated article at a pressure of
14.7 pounds per square inch (psi) (101.3 kilopascals (kPa)) or
less, or 4.0 pounds per square inch (psi) (27.58 kilopascals (kPa))
or less, or 3.0 psi (20.68 kPa), or 2.0 psi (13.79 kPa), or 1.0 psi
(6.9 kPa), or 0.9 psi (6.21 kPa), or 0.8 psi (5.52 kPa), or 0.7 psi
(4.83 kPa), or 0.6 psi (4.14 kPa), or even 0.5 psi (3.45 kPa) or
less, and at a pressure of at least 0.4 psi (2.76 kPa), or at least
0.5 psi (3.45 kPa).
Advantageously, the laminated article of the present disclosure
sufficiently encapsulates the guanidine-functionalized perlite
particles and the first and second substrates maintain their
integrity, such that the laminated article provides a turbidity of
less than 0.2 nephelometric turbidity units (NTU), or less than
0.15 NTU, or less than 0.10 NTU, according to the Turbidity Test.
The Turbidity Test is an indicator of how much (if any) material
(e.g., fibers, and/or particles) from the guanidine-functionalized
perlite particles and/or the substrates could potentially be shed
during use of the laminated article. The Turbidity Test is
significant in particular when the fluid sample contacted with the
laminated article is intended to be used following the contact, for
instance, when the fluid sample is potable water. The Turbidity
Test is based on the "Standard for Hygienic Safety Evaluation of
Equipment and Protective Materials in Drinking Water," (standard
number GB/T 17219-1998) and is as follows: A 47 mm disk of a
laminated sample is placed in a 2.5 liter vacuum filtration
apparatus (with a side arm) and flushed continuously with DI water
for 30 minutes. The sample is then removed and placed in a glass
jar containing 70 mL DI water for 24 hours. Water sample aliquots
are analyzed for turbidity using a turbidimeter, such as a MICRO
100 TURBIDIMETER (available from HF scientific, Fort Myers, Fla.).
Out of the 70 mL sample 2 samples of 25 mL are used for turbidity
measurements. A volume of 70 mL of DI water serves as control.
In a fifth aspect, another method of detecting microorganisms or
target cellular analytes in a fluid sample is provided. The method
includes providing a plurality of guanidine-functionalized perlite
particles according to the second aspect (as described above) and
providing a fluid sample suspected of containing at least one
microorganism strain or target cellular analyte. The method further
includes contacting the fluid sample with the plurality of
guanidine-functionalized perlite particles such that at least a
portion of the at least one microorganism strain or target cellular
analyte is bound to the guanidine-functionalized perlite particles
and detecting the presence of the at least one bound microorganism
strain or bound target cellular analyte.
Contacting the fluid sample with the plurality of
guanidine-functionalized perlite particles typically comprises
dispersing at least a portion of the particles in the fluid sample.
Optionally, the guanidine-functionalized perlite particles and the
fluid sample are combined (using any order of addition) in any of a
variety of containers (optionally but preferably, a capped, closed,
or sealed container; more preferably, a capped test tube, bottle,
or jar). Suitable containers for use in carrying out the process of
the invention will be determined by the particular sample and can
vary widely in size and nature. For example, the container can be
small, such as a 10 microliter container (for example, a test tube)
or larger, such as a 100 milliliter to 3 liter container (for
example, an Erlenmeyer flask or a polypropylene large-mouth
bottle). The container and any other apparatus or additives that
contact the fluid sample directly can be sterilized (for example,
by controlled heat, ethylene oxide gas, hydrogen peroxide, or
radiation) prior to use, in order to reduce or prevent any
contamination of the sample that might cause detection errors. The
amount of guanidine-functionalized perlite particles that is
sufficient to capture or concentrate the microorganisms and/or
cellular analytes of a particular sample for successful detection
will vary (depending upon, for example, the nature and form of the
concentration agent and sample volume) and can be readily
determined by one skilled in the art. For example, 10 milligrams of
guanidine-functionalized perlite particles per milliliter of sample
can be useful for some applications.
If desired, contacting can be effected by passing the
guanidine-functionalized perlite particles at least once through a
fluid sample (for example, by relying upon gravitational settling
over a period of, for example, about 10 minutes). Contact can be
enhanced by mixing (for example, by stirring, shaking, or use of a
rocking platform) such that the particles of
guanidine-functionalized perlite repeatedly pass or settle through
a substantial portion of the fluid sample. For small volumes on the
order of microliters (typically less than 0.5 milliliter), mixing
can be rapid such as by vortexing or "nutation," for example as
described in U.S. Pat. No. 5,238,812 (Coulter et al.). For larger
volumes on the order of greater than or equal to 0.5 milliliters
(typically 0.5 milliliter to 3 liters), mixing can be achieved by
gently tumbling the particulate concentration agent and the sample
in an "end over end" fashion, for example as described in U.S. Pat.
No. 5,576,185 (Coulter et al.). Such tumbling can be accomplished,
for example, by means of a device configured to hold a test tube or
other type of reaction vessel and to slowly rotate the test tube or
vessel in an "end over end" manner. Contacting can be carried out
for a desired period (for example, for sample volumes of about 100
milliliters or less, up to about 60 minutes of contacting can be
useful; preferably, about 15 seconds to about 10 minutes or longer;
more preferably, about 15 seconds to about 5 minutes).
Thus, mixing (for example, agitation, rocking, or stirring) and/or
incubation (for example, at ambient temperature) are optional but
preferred, in order to increase microorganism contact with the
guanidine-functionalized perlite particles. In certain embodiments,
contacting includes both mixing (for example, for about 15 seconds
to about 5 minutes) and incubating (for example, for about 3
minutes to about 30 minutes) a microorganism-containing fluid
sample with guanidine-functionalized perlite particles. If desired,
one or more additives (for example, lysis reagents, bioluminescence
assay reagents, nucleic acid capture reagents (for example,
magnetic beads), microbial growth media, buffers (for example, to
disperse or extract a solid sample), microbial staining reagents,
washing buffers (for example, to wash away unbound material),
elution agents (for example, serum albumin), surfactants (for
example, TRITON X-100 nonionic surfactant available from Union
Carbide Chemicals and Plastics, Houston, Tex.), mechanical
abrasion/elution agents (for example, glass beads), and the like)
can be included in the combination of guanidine-functionalized
perlite particles and fluid sample.
Optionally, the method further comprises segregation of the
resulting microorganism-bound guanidine-functionalized perlite
particles. Such segregation preferably can be achieved by relying,
at least in part, upon gravitational settling (gravity
sedimentation; for example, over a time period of about 5 minutes
to about 30 minutes). In some cases, however, it can be desirable
to accelerate segregation (for example, by centrifugation or
filtration) or to use combinations of any of the segregation
methods.
The method can optionally further comprise separating the resulting
microorganism-bound guanidine-functionalized perlite particles and
the fluid sample. This can involve removal or separation of the
supernatant that results upon segregation. Separation of the
supernatant can be carried out by numerous methods that are
well-known in the art (for example, by decanting or siphoning, so
as to leave the microorganism-bound guanidine-functionalized
perlite particles at the bottom of the container or vessel utilized
in carrying out the process). The method can be carried out
manually (for example, in a batch-wise manner) or can be automated
(for example, to enable continuous or semi-continuous
processing).
The fluid sample can be provided from a variety of different types
of samples, including, but not limited to, medical, environmental,
food, feed, clinical, and laboratory samples, and combinations
thereof. Medical or veterinary samples can include, for example,
cells, tissues, or fluids from a biological source (for example, a
human or an animal) that are to be assayed for clinical diagnosis.
Environmental samples can be, for example, from a medical or
veterinary facility (e.g., rinsate from cleaning medical supplies,
such as lumened devices), an industrial facility (e.g., produced
water and cooling tower water), soil, a water source, a food
preparation area (food contact and non-contact areas), or a
laboratory. Examples of samples that can be used include beverages
(for example, juices, beers, or carbonated beverages), water
(including potable water), biological fluids, and the like.
Fluid samples obtained in the form of a liquid or in the form of a
dispersion or suspension of solid in liquid can be used directly,
or can be concentrated (for example, by centrifugation) or diluted
(for example, by the addition of a buffer (pH-controlled)
solution). Samples in the form of a solid or a semi-solid can be
extracted, if desired, by a method such as, for example, washing or
rinsing with, or suspending or dispersing in, a fluid medium (for
example, a buffer solution). Samples can be taken from surfaces
(for example, by swabbing or rinsing). Preferably, the sample is at
least a fluid (for example, a liquid, a gas, or a dispersion or
suspension of solid or liquid in liquid or gas).
Sample volume can vary, depending upon the particular application.
For example, for a diagnostic or research application, the volume
of the fluid sample can be as small as in the microliter range (for
example, 10 microliters or greater). When a filtering process is
used for potable water safety testing, the volume of the sample can
typically be in the milliliter to liter range (for example, 100
milliliters to 3 liters). In industrial or residential
applications, the volume can be up to tens of thousands of
liters.
If desired, one or more additives (for example, lysis reagents,
bioluminescence assay reagents, nucleic acid capture reagents (for
example, magnetic beads), microbial growth media, buffers (for
example, to moisten a solid sample), microbial staining reagents,
washing buffers (for example, to wash away unbound material),
elution agents (for example, serum albumin), surfactants (for
example, "TRITON X-100" nonionic surfactant available from Union
Carbide Chemicals and Plastics, Houston, Tex.), adsorption buffers,
and the like can be included in a combination of the fluid sample
and the guanidine-functionalized perlite particles, nonwoven
article, or laminated article after contacting.
A variety of microorganisms can be concentrated and detected by
using the nonwoven articles and methods of the disclosure,
including, for example, bacteria, fungi, yeasts, protozoans,
viruses (including both non-enveloped and enveloped viruses),
fungal spores, bacterial endospores (for example, Bacillus
(including Bacillus anthracia, Bacillus cereus, and Bacillus
subtilis) and Clostridium (including Clostridium botulinum,
Clostridium difficile, and Clostridium perfringens)), and the like,
and combinations thereof, such as gram-negative bacteria,
gram-positive bacteria, yeasts, fungi, and combinations thereof.
Target cellular analyte that can be concentrated and detected by
using the methods of the disclosure include nucleic acids,
proteins, adenosine triphosphate (ATP), or combinations
thereof.
The methods optionally further comprise passing the fluid sample
through a coarse filter prior to the contacting the fluid sample
with guanidine-functionalized perlite particles, a nonwoven
article, or a laminated article. The use of such a filter can
remove particulates from the fluid sample that might otherwise clog
the article or interfere with the contacting. Suitable coarse
filters include for example and without limitation, filters
comprising pore sizes of at least 1 micrometer, at least 5
micrometers, at least 10 micrometers, at least 25 micrometers, or
at least 50 micrometers.
In certain embodiments, the method further comprises washing the at
least one microorganism strain- or target cellular analyte-bound
laminated article, nonwoven article, or guanidine-functionalized
perlite particles, prior to detection. It has been discovered that
contaminants such as residual sample matrix can be removed from
without significant loss of the bound or captured microorganisms
and/or cellular analytes. In certain embodiments, washing includes
for instance and without limitation, rinsing with sterile deionized
water or bottled drinking water, or rinsing with aqueous salt or
buffer solutions. Washing the laminated article, nonwoven article,
or guanidine-functionalized perlite particles tends to remove
components that could otherwise interfere with detecting the
presence of the bound microorganisms and/or cellular analytes,
depending on the particular detection method employed.
In certain embodiments, detecting the bound microorganism strain-
or target cellular analyte-bound comprises placing the
guanidine-functionalized perlite particles, the laminated article,
or the nonwoven article in a receptacle that comprises a material
through which a detection signal can be detected, wherein the
receptacle contains at least one reagent. For instance, placing the
microorganism strain- or target cellular analyte-bound material in
contact with a reagent optionally includes placing the
guanidine-functionalized perlite particles, the laminated article,
or the nonwoven article in a receptacle configured to be
operationally connected to a luminometer, wherein the receptacle
contains at least one reagent. Hence, in such an embodiment,
detection is facilitated by disposing the receptacle in the
luminometer for measurement of light generated from reaction of the
bound microorganism strain and/or target cellular analyte with at
least one reagent. Similarly, the receptacle can be interfaced with
other types of equipment depending on the particular detection
method. In certain embodiments, placing the microorganism strain-
or target cellular analyte-bound guanidine-functionalized perlite
particles, laminated article, or nonwoven article in contact with a
reagent includes pushing the material into a receptacle containing
the at least one reagent. Nonlimiting examples of suitable
receptacles, for instance receptacles containing at least one
reagent, include the 3M CLEAN-TRACE Surface ATP Swab available from
3M Company (St. Paul, Minn.), the AQUASNAP ATP Water Test available
from Hygiena (Camarillo, Calif.), the ACCUPOINT 2 ATP Sanitation
Monitoring System available from Neogen Corporation (Lansing,
Mich.), and the PRO-CLEAN Rapid Protein Residue Test available from
Hygiena.
It has been discovered that microorganism strain and/or target
cellular analyte can be detected without requiring removal from
being captured by the guanidine-functionalized perlite particles,
laminated article, or nonwoven article. The ability to detect
microorganism strains and/or target cellular analytes attached to
the guanidine-functionalized perlite particles, laminated article,
or nonwoven article is advantageous because it decreases the number
of required method steps as compared to methods in which the
microorganism strains and/or target cellular analytes need to be
eluted from a material prior to detection. Further, the
guanidine-functionalized perlite particles, laminated article, or
nonwoven article concentrates the microorganism strains and/or
target cellular analytes into the volume of the material, which is
typically significantly smaller than the volume of the fluid
sample.
Microorganisms and/or cellular analytes that have been captured or
bound (for example, by adsorption, absorption, or by sieving) by
the guanidine-functionalized perlite particles, laminated article,
or nonwoven article can be detected by essentially any desired
method that is currently known or hereafter developed. Such methods
include, for example, culture-based methods, microscopy (for
example, using a transmitted light microscope or an epifluorescence
microscope, which can be used for visualizing microorganisms tagged
with fluorescent dyes) and other imaging methods, immunological
detection methods, and genetic detection methods. The detection
process following microorganism and/or cellular analyte capture
optionally can include washing to remove sample matrix components,
staining, boiling or using elution buffers or lysis agents to
release cellular analyte from the nonwoven article, or the
like.
Immunological detection is detection of an antigenic material
derived from a target organism, which is commonly a biological
molecule (for example, a protein or proteoglycan) acting as a
marker on the surface of bacteria or viral particles. Detection of
the antigenic material typically can be by an antibody, a
polypeptide selected from a process such as phage display, or an
aptamer from a screening process.
Immunological detection methods are well-known and include, for
example, immunoprecipitation and enzyme-linked immunosorbent assay
(ELISA). Antibody binding can be detected in a variety of ways (for
example, by labeling either a primary or a secondary antibody with
a fluorescent dye, with a quantum dot, or with an enzyme that can
produce chemiluminescence or a colored substrate, and using either
a plate reader or a lateral flow device).
Detection can also be carried out by genetic assay (for example, by
nucleic acid hybridization or primer directed amplification). The
captured or bound microorganisms can be lysed to render their
genetic material (e.g., cellular analytes) available for assay.
Lysis methods are well-known and include, for example, treatments
such as sonication, osmotic shock, high temperature treatment (for
example, from about 50.degree. C. to about 100.degree. C.), and
incubation with an enzyme such as lysozyme, glucolase, zymolose,
lyticase, proteinase K, proteinase E, and viral enolysins.
Many commonly-used genetic detection assays detect the nucleic
acids of a specific microorganism, including the DNA and/or RNA.
The stringency of conditions used in a genetic detection method
correlates with the level of variation in nucleic acid sequence
that is detected. Highly stringent conditions of salt concentration
and temperature can limit the detection to the exact nucleic acid
sequence of the target. Thus microorganism strains with small
variations in a target nucleic acid sequence can be distinguished
using a highly stringent genetic assay. Genetic detection can be
based on nucleic acid hybridization where a single-stranded nucleic
acid probe is hybridized to the denatured nucleic acids of the
microorganism such that a double-stranded nucleic acid is produced,
including the probe strand. One skilled in the art will be familiar
with probe labels, such as radioactive, fluorescent, and
chemiluminescent labels, for detecting the hybrid following gel
electrophoresis, capillary electrophoresis, or other separation
method.
Particularly useful genetic detection methods are based on primer
directed nucleic acid amplification. Primer directed nucleic acid
amplification methods include, for example, thermal cycling methods
(for example, polymerase chain reaction (PCR), reverse
transcriptase polymerase chain reaction (RT-PCR), and ligase chain
reaction (LCR)), as well as isothermal methods and strand
displacement amplification (SDA) (and combinations thereof;
preferably, PCR or RT-PCR). Methods for detection of the amplified
product are not limited and include, for example, gel
electrophoresis separation and ethidium bromide staining, as well
as detection of an incorporated fluorescent label or radio label in
the product. Methods that do not require a separation step prior to
detection of the amplified product can also be used (for example,
real-time PCR or homogeneous detection).
Bioluminescence detection methods are well-known and include, for
example, adensosine triphosphate (ATP) detection methods including
those described in U.S. Pat. No. 7,422,868 (Fan et al.).
Bioluminescence detection methods for ATP often include the known
luciferin-luciferase system in which luciferase enzyme catalyzes
the oxidation of luciferin in the presence of ATP and a divalent
cation (such as magnesium or calcium). Other luminescence-based
detection methods can also be utilized.
In many embodiments, detection comprises a culture-based detection
method, an imaging detection method, a fluorescence-based detection
method, a colorimetric detection method, an immunological detection
method, a genetic detection method, a bioluminescence-based
detection method, or a combination thereof.
Various embodiments are provided that include
guanidine-functionalized perlite particles, a nonwoven article, a
laminated article, and methods of detecting microorganisms or
target cellular analytes in a fluid sample.
Embodiment 1 is a nonwoven article including a) a fibrous porous
matrix and b) a plurality of guanidine-functionalized perlite
particles enmeshed in the fibrous porous matrix.
Embodiment 2 is the nonwoven article of embodiment 1, wherein the
fibrous porous matrix includes nonwoven fibers.
Embodiment 3 is the nonwoven article of embodiment 1 or embodiment
2, wherein the fibrous porous matrix includes polymeric fibers.
Embodiment 4 is the nonwoven article of any of embodiments 1 to 3,
wherein the polymeric fibers include a polyamide, a polyolefin, a
polysulfone, or a combination thereof. Embodiment 5 is the nonwoven
article of any of embodiments 1 to 4, wherein the fibrous porous
matrix includes a fibrillated polyolefin polymeric fiber.
Embodiment 6 is the nonwoven article of any of embodiments 1 to 5,
wherein the fibrous porous matrix further includes inorganic
fibers.
Embodiment 7 is the nonwoven article of embodiment 6, wherein the
inorganic fibers include glass fibers, ceramic fibers, or a
combination thereof.
Embodiment 8 is the nonwoven article of any of embodiments 1 to 7,
wherein the fibrous porous matrix consists essentially of nonwoven
fibers.
Embodiment 9 is the nonwoven article of any of embodiments 1 to 8,
wherein the nonwoven article includes 5 to 55 weight percent
guanidine-functionalized perlite particles based on a total dried
weight of the nonwoven article and 45 to 95 weight percent fibrous
porous matrix based on the total dried weight of the nonwoven
article.
Embodiment 10 is the nonwoven article of any of embodiments 1 to 9,
wherein the nonwoven article includes 20 to 50 weight percent
guanidine-functionalized perlite particles based on a total dried
weight of the nonwoven article and 50 to 80 weight percent fibrous
porous matrix based on the total dried weight of the nonwoven
article.
Embodiment 11 is the nonwoven article of any of embodiments 1 to
10, wherein the fibrous porous matrix is a nonwoven fibrous layer
including polymeric fibers and inorganic fibers.
Embodiment 12 is the nonwoven article of any of embodiments 1 to
11, wherein the fibrous porous matrix is a nonwoven fibrous layer
and the guanidine-functionalized perlite particles are distributed
throughout the nonwoven fibrous layer.
Embodiment 13 is the nonwoven article of embodiment 12, wherein the
nonwoven fibrous layer includes polyolefin fibers and glass
fibers.
Embodiment 14 is the nonwoven article of embodiment 13, wherein the
inorganic fibers and polymeric fibers have an average length of
less than 50 millimeters.
Embodiment 15 is the nonwoven article of any of embodiments 1 to
14, wherein the fibrous porous matrix is a nonwoven fibrous layer
including uncrimped polymeric fibers.
Embodiment 16 is the nonwoven article of any of embodiments 1 to
15, wherein each of the guanidine-functionalized perlite particles
includes a perlite particle that is modified with at least one
silane having the formula X.sub.3-nR.sup.a.sub.nSi--Y-G, wherein: n
is 0, 1, or 2; each R.sup.a, if present, is independently an alkyl,
aralkyl, or aryl; Y is a divalent group comprising an alkylene
having 2 to 20 carbons; G is a guanidine group of the formula
--NH--C(.dbd.NH)--NH.sub.2; and each X is independently alkoxy or
acyloxy.
Embodiment 17 is the nonwoven article of embodiment 16, wherein the
divalent group further comprises an arylene, oxy, --NH--, or a
combination thereof.
Embodiment 18 is the nonwoven article of embodiment 16 or
embodiment 17, wherein the divalent group is alkylene having 3 to 6
carbons.
Embodiment 19 is the nonwoven article of any of embodiments 16 to
18, wherein the guanidine group is the reaction product of a
primary amine and an O-methylisourea salt.
Embodiment 20 is the nonwoven article of any of embodiments 16 to
19, wherein the linker is 3-aminopropyltrimethoxysilane.
Embodiment 21 is the nonwoven article of any of embodiments 14 to
18, wherein the ligand is the reaction product of one or more
hydroxyl groups of the perlite particle with one or more reactive
groups of a silane coupling agent moiety of the ligand.
Embodiment 22 is the nonwoven article of any of embodiments 1 to
19, wherein the guanidine-functionalized perlite particles have a
surface nitrogen content of at least 2 atomic percent as measured
by x-ray photoelectron spectroscopy (XPS).
Embodiment 23 is the nonwoven article of any of embodiments 1 to
20, wherein the guanidine-functionalized perlite particles have a
surface nitrogen content of up to 12 atomic percent as measured by
x-ray photoelectron spectroscopy (XPS).
Embodiment 24 is the nonwoven article of any of embodiments 1 to
21, wherein the fibrous porous matrix has a thickness of between
0.15 millimeters and 1 millimeter.
Embodiment 25 is a guanidine-functionalized perlite particle
including a perlite particle that is modified with at least one
silane having the formula X.sub.3-nR.sup.a.sub.nSi--Y-G,
wherein: n is 0, 1, or 2; each R.sup.a, if present, is
independently an alkyl, aralkyl, or aryl; Y is a divalent group
comprising an alkylene having 2 to 20 carbons; G is a guanidine
group of the formula --NH--C(.dbd.NH)--NH.sub.2; and each X is
independently alkoxy or acyloxy.
Embodiment 26 is the guanidine-functionalized perlite particle of
embodiment 25, wherein the divalent group further comprises an
arylene, oxy, --NH--, or a combination thereof.
Embodiment 27 is the guanidine-functionalized perlite particle of
embodiment 25 or embodiment 26, wherein the divalent group is
alkylene having 3 to 6 carbons.
Embodiment 28 is the guanidine-functionalized perlite particle of
any one of embodiments 25 to 27, wherein the guanidine group is the
reaction product of a primary amine and an O-methylisourea
salt.
Embodiment 29 is the guanidine-functionalized perlite particle of
any one of embodiments 25 to 28, wherein the linker is
3-aminopropyltrimethoxysilane.
Embodiment 30 is the guanidine-functionalized perlite particle of
any one of embodiments 25 to 29, have a surface nitrogen content of
at least 2 atomic percent as measured by x-ray photoelectron
spectroscopy (XPS).
Embodiment 31 is the guanidine-functionalized perlite particle of
any one of embodiments 25 to 30, have a surface nitrogen content of
up to 12 atomic percent as measured by x-ray photoelectron
spectroscopy (XPS).
Embodiment 32 is a laminated article including: a) a first
substrate; b) a second substrate sealed to the first substrate
along at least a portion of a perimeter of the first substrate; and
c) a plurality of guanidine-functionalized perlite particles
disposed between the first substrate and the second substrate.
Embodiment 33 is the laminated article of embodiment 32, wherein
each of the guanidine-functionalized perlite particles includes a
perlite particle that is modified with at least one silane having
the formula X.sub.3-nR.sup.a.sub.nSi--Y-G. In the formula, n is 0,
1, or 2 and each R.sup.a, if present, is independently an alkyl,
aralkyl, or aryl. In the formula, Y is a divalent group comprising
an alkylene having 2 to 20 carbons, G is a guanidine group of the
formula --NH--C(.dbd.NH)--NH.sub.2, and each X is independently
alkoxy or acyloxy.
Embodiment 34 is the laminated article of embodiment 32 or
embodiment 33, wherein the first substrate and the second substrate
are independently selected from a spunbond polypropylene, a
spunbond polyamide, a spunbond blend of polyamide and polyester, a
spunbond polyethylene, a spunbond polyester, a spunbond
polybutylene terephthalate, and a spunbond polypropylene.
Embodiment 35 is the laminated article of any of embodiments 32 to
34, wherein the first substrate and the second substrate are
independently selected from a spunbond polypropylene and a spunbond
blend of polyamide and polyester.
Embodiment 36 is the laminated article of any of embodiments 32 to
35, wherein the first substrate and the second substrate
independently include a spunbond material having a gram per square
meter basis weight (gsm) of 10 to 200 gsm, inclusive.
Embodiment 37 is the laminated article of any of embodiments 32 to
36, wherein the first substrate and the second substrate
independently include a spunbond material having a gram per square
meter basis weight (gsm) of 55 to 100 gsm, inclusive.
Embodiment 38 is the laminated article of any of embodiments 32 to
37, wherein the first substrate and the second substrate
independently include a spunbond material having a fiber diameter
of 10 to 30 micrometers (.mu.m), inclusive.
Embodiment 39 is the laminated article of any of embodiments 32 to
38, wherein the first substrate and the second substrate include
the same material.
Embodiment 40 is the laminated article of any of embodiments 32 to
39, wherein the second substrate is sealed to the first substrate
along up to 100% of the perimeter of the first substrate.
Embodiment 41 is the laminated article of any of embodiments 32 to
40, wherein the laminated article provides a turbidity of less than
0.2 nephelometric turbidity units (NTU) according to the Turbidity
Test.
Embodiment 42 is the laminated article of any of embodiments 32 to
41, wherein the first substrate includes a circular shape or a
polygon shape.
Embodiment 43 is the laminated article of any of embodiments 32 to
42, wherein at least one of the first substrate and the second
substrate includes a hydrophilized substrate.
Embodiment 44 is the laminated article of any of embodiments 32 to
43, wherein each of the first substrate and the second substrate is
liquid permeable.
Embodiment 45 is a method of detecting microorganisms or target
cellular analytes in a fluid sample. The method includes a)
providing a laminated article according to any one of embodiments
32 to 44; b) providing a fluid sample suspected of containing at
least one microorganism strain or target cellular analyte; c)
contacting the fluid sample with the laminated article such that at
least a portion of the at least one microorganism strain or target
cellular analyte is bound to the laminated article; and d)
detecting the presence of the at least one bound microorganism
strain or bound target cellular analyte.
Embodiment 46 is a method of detecting microorganisms or target
cellular analytes in a fluid sample. The method includes a)
providing a plurality of guanidine-functionalized perlite particles
according to any one of embodiments 25 to 31; b) providing a fluid
sample suspected of containing at least one microorganism strain or
target cellular analyte; c) contacting the fluid sample with the
plurality of guanidine-functionalized perlite particles such that
at least a portion of the at least one microorganism strain or
target cellular analyte is bound to the guanidine-functionalized
perlite particles; and d) detecting the presence of the at least
one bound microorganism strain or bound target cellular
analyte.
Embodiment 47 is the method of embodiment 45 or embodiment 46,
wherein the detecting includes a culture-based method, an imaging
method, an immunological detection method, a genetic detection
method, a bioluminescence method, or a combination thereof.
Embodiment 48 is the method of any of embodiments 45 to 47, wherein
the detecting includes a bioluminescence method.
Embodiment 49 is the method of any of embodiments 45 to 48, further
including contacting the at least one bound microorganism strain
with a lysis agent.
Embodiment 50 is the method of any of embodiments 45 to 49, wherein
the bound target cellular analyte includes a nucleic acid, a
protein, a cell wall component, ATP, or a combination thereof.
Embodiment 51 is the method of any of embodiments 45 to 50, wherein
the bound target cellular analyte includes ATP.
Embodiment 52 is the method of embodiment 45, wherein the
contacting includes passing the fluid sample at least once through
the laminated article.
Embodiment 53 is the method of embodiment 45 or embodiment 52,
wherein the contacting includes passing the fluid sample through
the laminated article at a pressure of 4.0 pounds per square inch
(psi) (27.58 kilopascals (kPa)) or less.
Embodiment 54 is the method of embodiment 45 or embodiment 52,
wherein the contacting includes passing the fluid sample through
the laminated article at a pressure of 0.5 psi (3.4 kPa) or
less.
Embodiment 55 is the method of any of embodiments 45 to 54, wherein
the microorganism strain is selected from strains of bacteria,
fungi, protozoans, viruses, bacterial endospores, and combinations
thereof.
Embodiment 56 is the nonwoven article of any of embodiments 1 to
24, wherein the nonwoven article has a basis weight in the range of
about 150 to about 350 grams per square meter (g/m.sup.2).
EXAMPLES
Unless otherwise noted, all chemicals used in the examples can be
obtained from Sigma-Aldrich Corp. (Saint Louis, Mo.). Unless
otherwise specified, all microbiological supplies and reagents were
purchased as standard products from either Sigma-Aldrich or
VWR.
TABLE-US-00001 Material Vendor Fiber 1 - SHORT STUFF E380F ~0.7 mm
MiniFIBERS, Inc.; Johnson City, TN average length, 15 microns
diameter polyethylene fibers Fiber 2 - 6 denier 2 inches long
chopped nylon MiniFIBERS, Inc.; Johnson City, TN fibers Fiber 3 - 1
denier bi-component ethylene vinyl MiniFIBERS, Inc.; Johnson City,
TN acetate/polypropylene fibers Fiber 4 - long glass fibers
(MICRO-STRAND Johns Mansville; Denver, CO 106-475 Glass Fiberglas)
Schuller Inc. Perlite 4106 - perlite powder Dicaperl Minerals
Corporation, Crawfordsville, IN Perlite 4156 - perlite powder
Dicaperl Minerals Corporation, Crawfordsville, IN Perlite 476 -
perlite powder Dicaperl Minerals Corporation, Crawfordsville, IN DE
- diatomaceous earth particles Dicaperl Minerals Corporation,
Crawfordsville, IN Escherichia coli ATCC 11229 American Type
Culture Collection, Manassas, VA Staphylococcus aureus ATCC 6538
American Type Culture Collection, Manassas, VA DI Water - Deionized
filtered 18 megaohm Millipore; Waltham, MA water from a Milli-Q
Gradient System ATP free water - HYPURE Molecular biology Thermo
Fisher Scientific; Waltham, MA grade water, Catalog #SH30538.02
CLEAN-TRACE pure ATP standard - reagent 3M Company; Bridgend, UK
for bioluminescence assay CLEAN-TRACE lysis reagent - reagent for
3M Company; Bridgend, UK bioluminescence assay CLEAN-TRACE
luciferin-luciferase enzyme 3M Company; Bridgend, UK reagent -
reagent for bioluminescence assay Tryptic Soy Broth - DIFCO Tryptic
Soy Becton Dickenson; Sparks MD Broth, prepared at 3% according to
the manufacturer's instructions TSA plate - plates prepared
according to Becton Dickenson; Sparks MD manufacturer's
instructions with 3 wt % Tryptic Soy Agar powder PAC - 3M PETRIFILM
Aerobic Count Plates 3M Company; St. Paul MN BBL Buffer -
Butterfield's buffer, pH 7.2 .+-. VWR; West Chester, PA 0.2,
monobasic potassium phosphate buffer solution (VWR Catalog Number
83008-093) 3M CLEAN-TRACE NG luminometer 3M Company, Bridgend, UK
Cuvettes - Greiner Bio-One polystyrene 4 mL VWR; West Chester, PA
tubes Microfuge tubes - 1.5 mL BrandTech VWR; West Chester, PA
polypropylene tubes 0.22 micron filter - Whatman Catalog # GE
Healthcare Life Sciences; Pittsburgh, PA 111106
Preparation of Guanylated Perlite Particles
Example 1
A solution of 3-aminopropyltrimethoxysilane (17.9 g, 100 mmol)
dissolved in anhydrous methanol (85 mL) was treated with of
O-methylisourea hemisulfate (12.3 g, 50 mmol). The reaction mixture
was stirred under an atmosphere of nitrogen overnight. A portion of
this solution (50 g) was transferred to a 500 mL round bottom flask
and diluted with 200 mL of anhydrous methanol. Perlite 4106
particles (50 g) were then added to the flask followed by the
addition of DI water (0.9 mL, 50 mmol). The mixture was stirred
rapidly for three days to facilitate reaction between the
trimethoxysilane and the particles. The resulting
guanidine-functionalized perlite particles were isolated by
filtration, rinsed with methanol, followed by water, and allowed to
air dry. The particles were then dried in a vacuum oven at
70.degree. C. overnight. The percent nitrogen content as measured
by ECSA is shown in Table 1 below.
TABLE-US-00002 TABLE 1 Surface composition of
guanidine-functionalized perlite particles by XPS avg. stdev.
Sample Rep C N O F Na Al Si S K Ca Fe Ag % N % N perlite A 5.8 0.0
64 0.2 2.1 3.5 22 0.0 1.9 0.1 0.03 0.00 0.1 0.10 perlite B 5.8 0.2
64 0.2 1.9 3.6 22 0.0 2.3 0.1 0.10 0.00 perlite C 5.3 0.1 64 0.2
2.2 3.5 22 0.0 2.3 0.1 0.06 0.00 g-perlite A 11 6.2 57 0.2 1.1 2.8
20 0.5 1.0 0.1 0.03 0.00 5.9 0.35 g-perlite B 11 5.8 57 0.5 1.3 2.9
20 0.4 0.9 0.1 0.07 0.00 g-perlite C 10 5.5 58 0.6 1.1 2.9 20 0.5
1.0 0.1 0.02 0.01
Testing of Guanylated Perlite for ATP Capture
Example 2
12 mg each of guanidine-functionalized perlite powder (of Example
1) and untreated perlite (Comparative Example 1, CE 1) were
aliquoted in cuvettes. A stock of ATP spiked water sample
containing the ATP standard was prepared such that each milliliter
of sample would contain 3000 RLUs ATP signal (about 7 microliters
of ATP standard per milliliter of water). To the cuvette tubes, 1
milliliter of spiked sample was added, the tubes were capped, and
the tubes were set on a rotating platform (Thermolyne VARI MIX
rocking platform (Barnstead International, Iowa) at 14
cycles/minute for 10 minutes. Next, the tubes were put in test tube
stands to settle the powder for 10 minutes. Supernatant samples
were removed into another cuvette, of which 100 microliters were
removed and tested for ATP assay.
A volume of 300 microliters of luciferase enzyme was added to the
cuvette containing the settled powder. The contents were mixed by
vortexing for 5 seconds, then the cuvette was connected to the
adaptor (custom made 12 centimeters (cm) long, 1 cm in diameter
made from DELRIN material) and read in the NG luminometer.
Similarly, a volume of 300 microliters of luciferase enzyme was
added to the cuvette and mixed on a vortex mixer for 10 seconds.
The cuvette was connected to an adaptor and read in the NG
luminometer. Supernatants were analyzed for mass balance purposes.
A 100 microliter volume from the spiked stock was tested for ATP
signal, which was multiplied by 10 to account for the 1 milliliter
test sample. The average total ATP signal in RLUS per 1 ml sample
was 318.75.times.10=3187.5 RLUs=3188 RLUs. % ATP Capture=(RLUs from
settled powder/RLUs from 1 ml spiked sample).times.100 The results
are reported in Table 2 below.
TABLE-US-00003 TABLE 2 Ave ATP signal Sample (in RLUs) % ATP
Capture 1 ml ATP spiked sample 3188 N/A Example 2 - powder 2278
71.45% Example 2 - supernatant 307 9.61% CE 1 - powder 22 0.69% CE
1 - supernatant 2277 71.41% N = 3, standard deviation <10%
unless noted
The same testing was set up with perlite powders with 1 ml water
(no ATP) as a background control. The background ATP signal for the
guanidine-functionalized powder of Example 1 was 2.3 RLUS, whereas
for the perlite powder of CE 1 it was 3.6 RLUS.
Preparation of Fibrous Porous Matrices Containing Guanylated
Perlite
Examples 3 and 4
Two fiber premixes were prepared by mixing various amounts of Fiber
1, Fiber 2, Fiber 3, and Fiber 4 as shown in Table 3 below. The
fibers were added to 3 liters of cold deionized water in a 4 L
blender (available from VWR, Radnor, Pa., under the trade
designation "WARING COMMERCIAL HEAVY DUTY BLENDER, MODEL 37BL84")
and blended at low speed for 30 seconds. The mixture was examined
for uniform dispersion of the fibers without nits or clumps. The
guanidine-functionalized perlite particles from Example 1 were
added with an additional liter of deionized water and mixed at low
speed for 15 seconds.
A nonwoven fibrous porous felt was prepared using a pad maker
apparatus (obtained from Williams Apparatus, Watertown, N.Y., under
the trade designation "TAPPI") that had a box measuring about 30
centimeters (12 inches) square and 30 centimeters (12 inches) high
with a fine mesh screen at the bottom and a drain valve. On the
screen .about. a 14 inch.times.12 inch piece of a polyethylene
spunbond (PET Lutradur 7240 obtained from Fiberweb, Cincinnati,
Ohio) was laid as scrim on the screen. The box was filled with tap
water up to a height of about 1 centimeter above the screen. Each
fiber and additive mixture was poured into the box and the valve
was opened immediately which created a vacuum that pulled the water
out of the box.
The fibrous porous felt was transferred from the apparatus onto a
20 centimeter square sheet of blotter paper (96-pound white paper,
obtained from Anchor Paper, St. Paul, Minn.). The fibrous porous
felt was sandwiched between 2 to 4 layers of blotter paper, to blot
excess water. The pressed fibrous porous felt was then transferred
onto a fresh sheet of blotter paper and placed in an oven (obtained
from SPX Thermal Product Solutions, White Deer, Pa., under the
trade designation "BLUE M STABIL-THERM OVEN, MODEL OV-560A2") set
at 110.degree. C. for about 3 hours to remove residual water and to
form a nonwoven fibrous porous matrix. The resulting fibrous porous
matrix of Example 3 was approximately 0.8-1 millimeter thick, while
the fibrous porous matrix of Example 4 was 0.5-0.8 mm thick.
TABLE-US-00004 TABLE 3 Material (grams) Example 3 Example 4 Fiber 1
11.16 8.87 Fiber 2 3.04 2.47 Fiber 3 2.33 1.85 Fiber 4 1.77 1.45
g-perlite 5.01 4.02 Basis weight 244.89 195.55 (g/m.sup.2)
Testing of Fibrous Porous Matrix with Guanylated Perlite for E.
coli and S. aureus Bacterial Capture and ATP Detection
A single colony from a streak culture of E. coli (ATCC 51813, a
Gram negative organism) was inoculated into 10 ml of TSB (Tryptic
Soy Broth, 3% by weight from Difco) and incubated overnight for
about 20 hours at 37.degree. C. The resulting bacterial stock
contained about 1.times.10.sup.9 cfus/ml. That stock was serially
diluted in DI water to make a working stock of 1.times.10.sup.5
cfus/ml.
14 mm disks of the fibrous porous matrix of Example 3 were die
punched and inserted into 13 mm filter holders (SWINNEX holders
obtained from Millipore). One ml of the above working stock of E.
coli was filtered through each disk using a 1 cc syringe. The
filtrate was discarded. Each disk was removed from the holder and
placed in a cuvette. A volume of 100 microliters of the lysis
reagent was added to the disk and vortexed for 10 seconds. A volume
of 300 microliters of luciferase enzyme was added to the cuvette
and vortexed for 10 seconds. The cuvette was connected to the
adaptor (custom made in 3M machine shop, 12 cm long, 1 cm in
diameter, made from DELRIN material) and read in the NG
luminometer. Disks through which 1 ml of unspiked DI water was
filtered were also tested, for background ATP signal. Another set
of disks was prepared, to which a 100 microliter volume from a
1.times.10.sup.5 cfus/ml dilution was spiked. This spiked disk was
tested for ATP signal (in RLUs) and was the "100% control" sample.
14 mm disks from the fibrous porous matrix of Example 4 were also
tested as described for the matrices of Example 3. Capture
efficiency was calculated using the formula below. The results are
shown in Table 4. % Capture Efficiency=(RLUs from test fibrous
porous matrix disk/RLUs from the 100% Control).times.100
TABLE-US-00005 TABLE 4 % Capture Example Sample ATP signal (in
RLUs) Efficiency N/A 100% Control for Matrix 1653 (39%) N/A of
Example 3 Example 5 Matrix of Example 3 1105 67 (40%) N/A 100%
Control for 1932 (3%) N/A Matrix of Example 4 Example 6 Matrix of
Example 4 1632 85 n = 2, % standard deviation indicated in
parentheses if greater than 10%. The background ATP signal for the
matrices of Examples 3 and 4 was 348 RLUs and 175 RLUs,
respectively, and was subtracted from the signal of the spiked
disks.
Capture and detection of S. aureus (ATCC 6538, a Gram positive
organism) using the fibrous porous matrices of Examples 3 and 4
were performed according to the method described above for E. coli.
The results are shown in Table 5 below.
TABLE-US-00006 TABLE 5 ATP signal Matrix Sample (in RLUs) % Capture
Efficiency N/A 100% Control 1785 (35%) N/A for Example 7 Example 3
Example 7 987 55 (21%) N/A 100% 1260 (23%) N/A Control for Example
8 Example 4 Example 8 768 61 (21%) n = 2, % standard deviation
indicated in parentheses if greater than 10%. The background ATP
signal for Examples 7 and 8 were 348 RLUS and 175 RLUS,
respectively, and were subtracted from the signal of the spiked
matrices.
Preparation of Guanylated Diatomaceous Earth
Comparative Example 3
50 g of diatomaceous earth particles were guanylated according to
the method described above according to Example 1, except that a 48
g portion of the reaction mixture solution was transferred to a 500
ml round bottom flask and diluted with 200 ml of anhydrous methanol
(instead of a 50 g portion). The particles were dried in a vacuum
oven at 70.degree. C. overnight to give 47 g of
guanidine-functionalized diatomaceous earth. The % nitrogen content
as measured by ECSA is shown in Table 6 below.
TABLE-US-00007 TABLE 6 XPS Surface Concentrations (Atomic %) avg.
stdev. Sample Rep C N O F Na Al Si S K Ca Fe Ag % N % N perlite A
5.8 0.0 64 0.2 2.1 3.5 22 0.0 1.9 0.1 0.03 0.00 0.1 0.10 perlite B
5.8 0.2 64 0.2 1.9 3.6 22 0.0 2.3 0.1 0.10 0.00 perlite C 5.3 0.1
64 0.2 2.2 3.5 22 0.0 2.3 0.1 0.06 0.00 g-perlite A 11 6.2 57 0.2
1.1 2.8 20 0.5 1.0 0.1 0.03 0.00 5.9 0.35 g-perlite B 11 5.8 57 0.5
1.3 2.9 20 0.4 0.9 0.1 0.07 0.00 g-perlite C 10 5.5 58 0.6 1.1 2.9
20 0.5 1.0 0.1 0.02 0.01 diatom. earth A 4.9 0.1 65 1.2 1.9 3.2 22
0.0 1.5 0.1 0.09 0.00 0.2 0.11 diatom. earth B 4.9 0.2 65 1.2 1.9
3.2 22 0.0 1.6 0.1 0.11 0.00 diatom. earth C 4.1 0.3 65 1.1 2.0 3.2
23 0.0 1.7 0.1 0.09 0.00 g-d.e. A 10 5.7 57 0.4 1.3 2.8 21 0.7 1.1
0.0 0.10 0.03 5.4 0.24 g-d.e. B 9.5 5.2 58 0.4 1.2 2.9 21 0.6 1.1
0.1 0.09 0.01 g-d.e. C 9.5 5.4 58 0.4 1.1 2.7 21 0.6 1.1 0.1 0.11
0.02
Testing of Guanylated DE for ATP Capture
12 mg each of guanidine-functionalized diatomaceous earth (DE)
powder of Comparative Example 3 (CE 3) and untreated DE powder
(Comparative Example 4, CE 4) were aliquoted in cuvettes. A stock
of ATP spiked water sample containing ATP standard was prepared
such that each ml of sample would contain 3000 RLUs ATP signal (32
microliters of ATP standard per ml water). The test was performed
as described in Example 2 above. The average total ATP signal in
RLUS per 1 ml sample was 240.times.10=2400 RLUs. % ATP
Control=(RLUs from settled powder/RLUs from 1 ml spiked
sample).times.100. The results are shown in Table 7 below.
TABLE-US-00008 TABLE 7 Ave ATP signal Sample (in RLUs) % ATP
Control 1 ml ATP spiked sample 2400 100% CE 3 - powder 151 6.29 CE
3 - supernatant 385 16 (12%) CE 4 - powder 4.25 0.18 CE 4 -
supernatant 1500 63 (12%) N = 2, standard deviation <10% unless
noted in parentheses
The same testing was set up with DE powders, with 1 ml water
(containing no ATP) as a background control. The background ATP
signal for the guanidine-functionalized DE powder of CE 3 was 6
RLUs, whereas for the DE powder of CE 4 it was 4.5 RLUs.
Preparation of Guanylated Perlite 476 and 4156
Examples 9 and 10
Perlite 476 particles and perlite 4156 particles (50 g each) were
guanylated as described above in Example 1, except that 48 g of the
reaction mixture solution was transferred to a 500 ml round bottom
flask and diluted with 200 ml of anhydrous methanol (instead of a
50 g portion). The particles were then dried in a vacuum over at
60.degree. C. overnight to give 49 g each of
guanidine-functionalized perlite 476 particles (Example 9) and
guanidine-functionalized perlite 4156 particles (Example 10. The %
nitrogen content as measured by ECSA is shown in Table 8 below.
TABLE-US-00009 TABLE 8 XPS Surface Concentrations (Atomic %) Sample
Area C N O F Na Al Si S K Ca Fe perlite 476 control A 7.2 0.0 62
0.0 2.1 3.5 23 0.0 2.1 0.1 0.05 perlite 476 control B 7.3 0.0 62
0.1 1.8 3.3 23 0.0 2.0 0.1 0.11 perlite 476 control C 6.9 0.0 62
0.0 2.1 3.5 23 0.0 2.4 0.1 0.11 g-perlite 476 A 12 5.6 55 0.3 1.3
3.0 21 0.5 1.2 0.1 0.14 g-perlite 476 B 12 5.6 55 0.3 1.2 2.9 21
0.5 1.0 0.1 0.04 g-perlite 476 C 11 5.2 56 0.4 1.2 3.2 21 0.4 1.3
0.1 0.21 perlite 4156 control A 6.7 0.1 62 0.3 2.1 3.6 23 0.0 2.2
0.1 0.01 perlite 4156 control B 6.4 0.1 62 0.3 2.1 3.7 23 0.0 2.3
0.1 0.00 perlite 4156 control C 6.0 0.1 62 0.3 1.9 3.6 23 0.0 2.5
0.1 0.16 g-perlite 4156 A 10 4.2 57 0.4 1.3 3.3 22 0.3 1.3 0.1 0.09
g-perlite 4156 B 10 4.6 57 0.4 1.1 3.3 22 0.4 1.3 0.1 0.21
g-perlite 4156 C 10 4.4 57 0.3 1.4 3.2 22 0.4 1.4 0.1 0.10
Testing of Guanylated Perlite 476 and Perlite 4156 for ATP
Capture
Examples 11 and 12
12 mg each of the powder of guanidine-functionalized perlite 476
(Example 11), untreated Perlite 476 (Comparative Example 5, CE 5),
guanidine-functionalized perlite 4156 (Example 12), and untreated
Perlite 4156 (Comparative Example 6, CE 6) were aliquoted in
cuvettes. A stock of ATP spiked water sample containing the ATP
standard was prepared such that each ml of sample would contain
3000 RLUs ATP signal (32 microliters of ATP standard per ml water).
The test was performed as described in Example 2 above. The average
total ATP signal in RLUs per 1 ml sample was 240.times.10=2400
RLUs. % ATP Control=(RLUs from settled powder/RLUs from 1 ml spiked
sample).times.100. The results are shown in Table 9 below.
TABLE-US-00010 TABLE 9 Ave ATP signal Sample (in RLUs) % ATP
Control 1 ml ATP spiked sample 2400 100 perlite 476 powder (CE 5)
10 0.6 (81%) perlite 476 supernatant 1510 63 (CE 5 supernatant)
g-perlite 476 powder 1596 67 g-perlite 476 supernatant 165 7 (56%)
perlite 4156 powder (CE 6) 10 0.6 (82%) perlite 4156 supernatant
(CE 6 2025 84 supernatant) g-perlite 4156 powder 1602 68 g-perlite
4156 supernatant 110 5 N = 2, standard deviation <10% unless
noted in parentheses
The same testing was set up with powders with 1 ml water
(containing no ATP) as a background control. The background ATP
signal for guanidine-functionalized perlite 476 powder was 40 RLUs,
CE 5 was 7 RLUs, guanidine-functionalized perlite 4156 powder was
41 RLUs, and CE 6 was 4 RLUs. The background signals for
guanidine-functionalized perlite 476 and 4156 were subtracted from
the ATP capture signal.
Testing of Example 3 for Rapid Microbial Monitoring in Produced
Water Samples
Produced water samples were obtained from an oil well in Canada.
Samples were serially diluted in BBL buffer and plated 1 ml each on
PAC plates. The plates were incubated at 37.degree. C. for 48
hours, per manufacturer instructions. The plates were analyzed for
bacterial counts using the 3M PETRIFILM Plate Reader. A one hundred
microliter volume from each sample was added to a cuvette and mixed
with 145 microliters of the CLEAN-TRACE Water-Plus Total ATP
extractant and vortexed for 10 seconds. A volume of 450 microliters
of the CLEAN-TRACE Water-Plus Total ATP enzyme was added, then
mixed for 10 seconds. Using an adaptor (described above with
respect to Examples 5 and 6) the cuvette was inserted into the NG
luminometer to measure the ATP signal.
Based on the volumes filtered, colony counts and ATP values, two
samples were further selected for microbial testing with the
nonwoven fibrous porous matrices of Example 3. Sample E
(Comparative Example 8, CE 8) had approximately 3.times.10.sup.2
cfus/ml, a free (non-microbial) ATP signal of 25 RLUs, and a total
ATP signal of 46 RLUs. Sample G (Comparative Example 9, CE 9) had
4.7.times.10.sup.5 cfus/ml, a free (non-microbial) ATP signal of 39
RLUs, and a total ATP signal of 315 RLUs.
A 10 ml volume from each produced water sample was processed
through 14 mm disks of the fibrous porous matrix of Example 3 and
0.22 micron filter (Comparative Example 7, CE 7) to evaluate
filtration capability. Filtration was terminated once flow through
stopped due to clogging. The volumes prior to clogging are shown in
Table 10 below.
TABLE-US-00011 TABLE 10 Produced Water Volume through CE 7 Volume
through sample # (in ml) Example 3 (in ml) Sample A 10 10 Sample B
2 10 Sample C 0.5 10 Sample D 4.5 10 Sample E 0.5 10 Sample F 1 10
Sample G 10 10 Sample H 10 10
14 mm disks of the nonwoven fibrous porous matrix of Example 3 were
die punched and inserted into 13 mm filter holders (SWINNEX holders
obtained from Millipore). Ten ml of produced water sample E was
filtered through a disk using a 10 cc syringe. The filtrate was
discarded. The disk was removed from the holder and tested for the
ATP signal as described above for produced water samples. A second
disk was processed the same, except that it was washed with 10 ml
DI water prior to analysis for the ATP signal.
Fibrous porous matrix disks through which 10 ml of unspiked DI
water was filtered were tested for background ATP signal. The
background signal was 253 RLUs and was subtracted from test
readings. The improvement in ATP signal from captured bacteria over
a CLEAN-TRACE test (without concentrating the bacteria in a
nonwoven fibrous porous matrix) was calculated using the formula
below. The results are shown in Table 11 below.
The fold increase in ATP signal over a CLEAN-TRACE test (without
concentrating the bacteria in a nonwoven fibrous porous
matrix)=(RLUs from post filtration wet-laid disk/RLUs from 100
microliters of unfiltered sample).
Free (non-microbial) ATP content in CE 8 and in disks of the matrix
of Example 3 (washed and not washed) was analyzed by using 450
microliters of the CLEAN-TRACE Water-Plus Total ATP enzyme, mixing
for 10 seconds, and reading the ATP signal in the NG
luminometer.
TABLE-US-00012 TABLE 11 Fold increase Produced Ave Free ATP Ave
Total over current Water signal (in ATP signal test in Total Matrix
sample RLUs) (in RLUs) ATP Example 3 E 27 (93) 3408 (52) 61 (not
washed) Example 3 E 6507 (86) 71613 1279 (washed) CE 8 E 25 (73) 56
(35) N/A Example 3 G 883 11653 37 (not washed) Example 3 G 624 (22)
23578 72 (washed) CE 9 G 39 (13) 315 N/A N = 2, standard deviation
less than 10% unless otherwise noted in parentheses
Comparative Examples 8 and 9 were evaluated for turbidity using a
Micro 100 Turbidimeter. DI water was used a reference standard. CE
8 had an average turbidity of 138 NTUs and CE 9 had an average
turbidity of 0.96, while DI water had a turbidity of 0.02 NTUs.
Example CE 8 had to be diluted 4 fold in DI water in order to get
the measurements. Thus, the reported turbidity for CE 8 is 4 times
the actual measurement (4.times.34.5).
The variation in tests suggests matrix interference. The
improvement in ATP signal after washing indicates the decrease in
carryover of inhibitory substances, which allows the ATP assay to
be used for rapid monitoring of produced water samples following
washing.
Guanylated Perlite Immobilized within Spunbond Scrims (Prophetic
Example)
A spunbond substrate with an average pore size less than the
average pore size of the guanidine-functionalized particles of
Example 1 is laid flat on a clean bench. A 16 mm diameter circular
area is marked on the substrate. A 15 mg aliquot of the material of
Example 1 is weighed out and placed on the marked area. This is
repeated three times to make three replicate samples. Another sheet
of a spunbond substrate is laid flat on top of the areas with the
weighed powder. The top sheet is carefully flattened. The marked
area is ultrasonically welded using a BRANSON 2000d ULTRASONIC
WELDER. The ultrasonic horn has an outer diameter of 18 mm and an
inner diameter of 16 mm. The welding is performed on a flat
aluminum plate at a setting of 250 Joules.
The welded laminated articles are cut off using scissors and placed
into Swinnex holders for ATP capture studies as described above in
Example 2. Briefly, one milliliter of DI water is spiked with 3000
RLUs ATP and is filtered through the laminated article using a 1 cc
syringe. After filtration the laminated article is removed from the
filter holder and added to a cuvette. 145 microliters of the
CLEAN-TRACE Water-Plus Total ATP extractant is added to the
cuvette. The cuvette is vortexed for 10 seconds. A volume of 450
microliters of the CLEAN-TRACE Water-Plus Total ATP enzyme is
added, then mixed for 10 seconds. The cuvette is connected to the
adaptor (as described in Example 2 above) and is read in the NG
luminometer.
Laminated articles are also tested for background signal by
filtering one ml of unspiked deionized water through them. The
background signal is subtracted from the test signal. A one hundred
microliter aliquot of the stock ATP solution is tested to generate
a signal that is multiplied by 10 to generate a "100% Control"
signal. % ATP Control=(RLUs from laminated article/RLUs from 1 ml
spiked sample).times.100.
While the specification has described in detail certain exemplary
embodiments, it will be appreciated that those skilled in the art,
upon attaining an understanding of the foregoing, may readily
conceive of alterations to, variations of, and equivalents to these
embodiments. Furthermore, all publications and patents referenced
herein are incorporated by reference in their entirety to the same
extent as if each individual publication or patent was specifically
and individually indicated to be incorporated by reference. Various
exemplary embodiments have been described. These and other
embodiments are within the scope of the following claims.
* * * * *
References